WO2014192104A1 - Information processing device and method, and program - Google Patents

Information processing device and method, and program Download PDF

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Publication number
WO2014192104A1
WO2014192104A1 PCT/JP2013/064930 JP2013064930W WO2014192104A1 WO 2014192104 A1 WO2014192104 A1 WO 2014192104A1 JP 2013064930 W JP2013064930 W JP 2013064930W WO 2014192104 A1 WO2014192104 A1 WO 2014192104A1
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WO
WIPO (PCT)
Prior art keywords
risk
result
sample
degree
safety
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PCT/JP2013/064930
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French (fr)
Japanese (ja)
Inventor
吉田 伸一
Original Assignee
株式会社らいふ
一般社団法人食の安心安全推進国際センター機構
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by 株式会社らいふ, 一般社団法人食の安心安全推進国際センター機構 filed Critical 株式会社らいふ
Priority to PCT/JP2013/064930 priority Critical patent/WO2014192104A1/en
Priority to JP2015519548A priority patent/JP6106863B2/en
Priority to SG11201509684XA priority patent/SG11201509684XA/en
Publication of WO2014192104A1 publication Critical patent/WO2014192104A1/en

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    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06QINFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
    • G06Q10/00Administration; Management
    • G06Q10/06Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling

Definitions

  • the present invention relates to an information processing apparatus and method, and a program, and more particularly to an information processing apparatus and method, and a program capable of providing an index that can comprehensively determine the degree of safety against health damage.
  • the present invention has been made in view of such a situation, and is intended to be able to provide an index that can comprehensively determine the degree of safety against health damage.
  • An information processing apparatus is An impact determination unit that determines the impact of risk on health damage; A frequency determination unit that determines the frequency of occurrence of the risk; The degree of safety is calculated by calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk It has a department and
  • An information processing method is Determine the impact of risk on health hazards, Determine the frequency of occurrence of the risk, Calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk .
  • the program according to one aspect of the present invention is On the computer Determine the impact of risk on health hazards, Determine the frequency of occurrence of the risk, The magnitude of the risk is calculated using the determined degree of influence of the risk and the frequency of occurrence of the risk, and the process of calculating the degree of safety against health damage from the magnitude of the calculated risk is performed.
  • the degree of risk impact on health damage is determined, the frequency of occurrence of the risk is determined, and the degree of impact of the risk determined and the frequency of occurrence of the risk are used to determine the risk.
  • the degree of safety against health damage is calculated from the calculated magnitude of the risk.
  • FIG. 1 is a block diagram showing a configuration example of a safety degree scale system to which the present invention is applied.
  • the safety scale system 1 of FIG. 1 is a system that inspects and evaluates safety (safety) of human health damage such as food poisoning, radiation, hygiene management, microbes, and the like.
  • the safety scale system 1 is used, for example, in elementary or junior high school, a factory, an office, a kitchen or cafeteria such as a nursing home, a restaurant store, a food factory, etc. Examine, evaluate and output.
  • the safety scale system 1 can centrally manage the hygiene status of many business sites, and is particularly useful when many business sites are deployed throughout the country or certain regions. It is. In the present embodiment, an example will be described in which the degree of safety of a product (food) manufactured and provided at each store is inspected at a chain store of a company that is expanding a restaurant chain.
  • the safety scale system 1 of FIG. 1 centrally manages the safety of products provided at a plurality of stores of a chain store of a company that is expanding a restaurant chain.
  • the security level scale system 1 is configured of a server 11 and one or more terminal devices 12. Although three terminal devices 12-1 to 12-3 are illustrated in FIG. 1, the number of terminal devices 12 can be increased or decreased as needed.
  • the server 11 and the terminal device 12 are connected by a network such as the Internet, a LAN (Local Area Network), or a VPN (Virtual Private Network).
  • the server 11 as an information processing apparatus that processes information for performing a safety degree inspection executes an application program (hereinafter, referred to as a safety degree inspection program) for performing a safety degree inspection.
  • a safety degree inspection program an application program for performing a safety degree inspection.
  • the terminal device 12 is, for example, a personal computer (including a notebook type), a tablet terminal, a high-performance mobile phone called a so-called smartphone, a dedicated input terminal, or the like.
  • the terminal device 12 is kept at each store or is carried by an investigator who patrols each store and investigates the hygiene condition and the like of the store.
  • a store manager such as a store manager of each store, a manager responsible for managing the sanitary condition of the company operating the store, or an investigator (hereinafter collectively referred to as a user) operates the terminal device 12 to operate the terminal device 12 accesses the server 11 on which the safety check program is executed.
  • the security level inspection program executed by the server 11 is, for example, a WEB application created in a markup language such as HTML, and a predetermined screen created by the security level inspection program is executed on the terminal device 12 It is displayed on the display of the terminal device 12 by the browser.
  • the browser for example, interprets an HTML (Hypertext Markup Language) document and displays a screen on a display or the like, or sets a URL (Uniform Resource Locators) to access the web site of the server 11 and access the data. It has basic functions such as a communication function that downloads or sends data to a site, or a jump function that jumps to a linked URL in an HTML document.
  • the terminal device 12 receives an operation (input) performed by the user on a predetermined screen displayed on the display by the safety level inspection program, and transmits the operated content to the server 11 via the network.
  • the server 11 on which the safety level inspection program is executed receives the content operated by the terminal device 12 and performs predetermined data processing according to the content operated, or the next screen is displayed on the terminal device 12. Or display it.
  • FIG. 2 shows an example of the hardware configuration of the server 11.
  • a central processing unit (CPU) 31 executes various processes in accordance with a program stored in a read only memory (ROM) 32 or a storage unit 38.
  • the program mentioned here includes, for example, an operating system (OS) such as Windows (registered trademark), a driver of a network adapter, and the like, as well as the above-described safety degree inspection program.
  • the RAM (Random Access Memory) 33 appropriately stores programs executed by the CPU 31, data, and the like.
  • the CPU 31, the ROM 32 and the RAM 33 are mutually connected by a bus 34.
  • the program executed by the CPU 31 (computer) of the server 11 may be a program that performs processing in chronological order according to the order described in this specification, or when calls are performed in parallel or in parallel. It may be a program that is individually processed at necessary timing such as.
  • An input / output interface 35 is also connected to the CPU 31 via the bus 34.
  • the input / output interface 35 is connected to an input unit 36 including a keyboard, a mouse, a microphone and the like, and an output unit 37 including a display, a speaker and the like.
  • the CPU 31 executes various processes in response to the command input from the input unit 36. Then, the CPU 31 outputs the result of the process to the output unit 37.
  • the input / output interface 35 is also connected to a storage unit 38 formed of, for example, a hard disk.
  • the storage unit 38 stores programs executed by the CPU 31 and various data. Note that this program may be acquired from an external device by the communication unit 39.
  • a communication unit 39 for communicating with an external device through a network and a drive 40 are connected to the input / output interface 35.
  • a removable medium 41 such as a magnetic disk, an optical disk, a magneto-optical disk, or a semiconductor memory
  • the drive 40 drives them and acquires programs and data recorded therein. The acquired program and data are transferred to and stored in the storage unit 38 as necessary.
  • the hardware configuration of the terminal device 12 of FIG. 1 is also basically the same as the configuration of the server 11, and thus the description thereof will be omitted.
  • FIG. 3 shows an example of a main screen displayed first on a display (browser) of the terminal device 12 when the user accesses the server 11 on which the safety level inspection program is executed from the terminal device 12. .
  • the main screen shown in FIG. 3 is classified into four groups of a basic information registration group, an examination result registration group, a survey result registration group, and a result browsing group.
  • the basic information registration group is a group for registering basic information such as a company name and a product name (specimen name) to be subjected to a safety inspection.
  • the basic information registration group includes a sample information registration button 61 and a customer master button 62.
  • the sample information registration button 61 is pressed (operated) by the user when registering a product to be inspected (hereinafter, also referred to as a sample).
  • a sample information registration screen of FIG. 5 described later is displayed.
  • the customer master button 62 is pressed by the user when registering customer information, such as a company to be inspected, facilities of the company or facilities of the company, and the like.
  • customer information such as a company to be inspected, facilities of the company or facilities of the company, and the like.
  • a customer registration screen for inputting a customer name and a facility name, a code number uniquely identifying them, and the like is displayed, and the contents registered on the customer registration screen are stored as a customer database. Be done.
  • the test result registration group is a group that registers (inputs) test results on the toxicity and medicine of the sample.
  • food poisoning bacteria result registration button 71 pesticide / antibiotic result registration button 72
  • radiation measurement result registration button 73 foreign substance contamination inspection result registration button 74
  • allergen contamination inspection result registration button 75 virus inspection
  • virus inspection A result registration button 76 is included.
  • the food poisoning bacteria result registration button 71 is pressed by the user when registering the test result of the food poisoning bacteria test of the sample.
  • a food poisoning bacteria test result registration screen of FIG. 6 described later is displayed.
  • the pesticide / antibiotic result registration button 72 is pressed by the user when registering the test result of the content of the pesticide / antibiotic of the sample.
  • the pesticide / antibiotic result registration button 72 is pressed, the pesticide / antibiotic test result registration screen of FIG. 7 described later is displayed.
  • the radiation measurement result registration button 73 is pressed by the user when registering the inspection result of the radiation dose of the sample.
  • a radiation measurement result registration screen of FIG. 11 described later is displayed.
  • the foreign substance contamination inspection result registration button 74 is pressed by the user when registering the inspection result of the foreign substance contamination inspection of the sample.
  • a foreign substance contamination inspection result registration screen of FIG. 12 described later is displayed.
  • the allergen contamination test result registration button 75 is pressed by the user when registering the test result of the allergen contamination test of the sample.
  • the allergen contamination test result registration button 75 is pressed, the allergen contamination test result registration screen of FIG. 13 described later is displayed.
  • the virus test result registration button 76 is pressed by the user when registering the test result of the norovirus test on the sample and the worker. When the virus test result registration button 76 is pressed, a virus test result registration screen of FIG. 14 described later is displayed.
  • the survey result registration group is a group that registers survey results on the hygiene of workers and facilities that handle specimens.
  • the survey result registration group includes a health management survey result registration button 81, an infection prevention countermeasure survey result registration button 82, a personal appearance / dress / hair style / decoration survey result registration button 83, and a hygiene education survey result registration button 84.
  • the health management survey result registration button 81 is pressed by the user when registering the result of survey on the worker regarding the level of health management managed by the individual.
  • a health management research result registration screen of FIG. 15 described later is displayed.
  • the infection prevention countermeasure research result registration button 82 is pressed by the user when registering the result of investigating the infection prevention countermeasure of the facility.
  • an infection prevention countermeasure research result registration screen of FIG. 16 described later is displayed.
  • the appearance / dress / haircut / decoration research result registration button 83 is pressed by the user when registering the result of investigation on the appearance / dress / haircut / decoration of the worker.
  • the appearance / dress / haircut / decoration research result registration button 83 is pressed, the appearance / dress / hairstyle / modification research result registration screen of FIG. 17 described later is displayed.
  • the hygiene education research result registration button 84 is pressed by the user when registering the research result on the health education system and the degree of understanding of the worker.
  • a hygiene education research result registration screen of FIG. 18 described later is displayed.
  • the result browsing group is a group that outputs the test results of the sample.
  • the result browsing group includes a result list button 91 and a result output button 92.
  • the result list button 91 is pressed by the user when displaying a list of examination / survey results of each examination item of the sample.
  • a result list screen of FIG. 19 described later is displayed.
  • the result output button 92 is pressed by the user when displaying the final safety determination result based on the examination result and the examination result of the sample.
  • the result output button 92 is pressed, the result output screen of FIG. 20 described later is displayed.
  • FIG. 4 is a block diagram showing an example of a functional configuration of the safety degree scale system 1 realized by the safety degree inspection program being executed by the server 11.
  • the safety degree scale system 1 includes a basic information registration unit 101, an examination result registration unit 102, a survey result registration unit 103, a risk influence degree judgment unit 104, a risk occurrence frequency judgment unit 105, a safety degree calculation unit 106, a result output unit 107. And a registration DB 108.
  • the basic information registration unit 101 executes processing when the sample information registration button 61 and the customer master button 62 belonging to the basic information registration group are pressed on the main screen of FIG. 3.
  • the examination result registration unit 102 belongs to the examination result registration group on the main screen of FIG. 3 and includes the food poisoning bacteria result registration button 71, the agrochemical / antibiotic result registration button 72, the radiation measurement result registration button 73, and the foreign matter contamination inspection result registration button 74, the processing when the allergen contamination test result registration button 75 and the virus test result registration button 76 are pressed is executed.
  • the survey result registration unit 103 belongs to a survey result registration group, and includes a health management survey result registration button 81, an infection prevention countermeasure survey result registration button 82, a personal appearance / dress / hair style / decorative survey result registration button 83, and a hygiene education survey result registration. A process when the button 84 is pressed is executed.
  • the risk influence degree determination unit 104 determines the degree of influence of the risk of the sample on the health damage based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Details of the method of determining the degree of risk influence will be described later.
  • the risk occurrence frequency determination unit 105 determines the occurrence frequency of the risk of the sample to the health damage based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Details of the method of determining the risk occurrence frequency will be described later.
  • the safety degree calculation unit 106 calculates the magnitude of the risk using the degree of impact of the risk determined by the risk degree of impact determination unit 104 and the occurrence frequency of the risk determined by the risk occurrence frequency determination unit 105, From the calculated magnitude of risk, calculate the degree of safety against health damage. Although the details will be described later, the degree of safety against health damage is calculated by the reciprocal of the calculated magnitude of risk.
  • the result output unit 107 executes processing when the result list button 91 and the result output button 92 belonging to the result browsing group are pressed on the main screen of FIG. 3.
  • the registration DB 108 stores information registered by the basic information registration unit 101, the inspection result registration unit 102, the survey result registration unit 103 and the like, and the result calculated by the safety degree calculation unit 106 and the like.
  • the customer database is one of the databases stored in the registration DB 108.
  • the basic information registration unit 101, the examination result registration unit 102, the investigation result registration unit 103, and the result output unit 107 are a display control unit for displaying a predetermined screen on the display of the server 11 and the terminal device 12, the server 11 and the terminal device
  • An information acquisition unit that acquires input information input from a keyboard, a mouse or the like 12 and a communication control unit that controls communication between the server 11 and the terminal device 12 are individually or commonly provided.
  • FIG. 5 shows an example of the sample information registration screen.
  • the user presses the sample information registration button 61 on the main screen of FIG. 3. Thereby, the sample information registration screen of FIG. 5 is displayed.
  • each item of customer name 121, facility name 122, facility CD 123, sub CD 124, sample name 125, sample ID 126, test 127, and survey 128, registration button 129, correction button 130, and cancel button 131 Is displayed.
  • the company name of the customer, the facility name of the store or business place, and the product name to be inspected are input by the user.
  • the name of the food to be tested such as "cake" is input.
  • the company name and facility name of the customer may be directly input, or based on the customer database input on the customer registration screen displayed when the customer master button 62 is pressed, the company name and facility name are selected and input by pull-down. It may be possible.
  • the item of the sample ID 126 is blank in the initial state of the sample information registration screen.
  • a sample ID is assigned by the basic information registration unit 101 and stored in the registration DB.
  • the correction button 130 When it is desired to correct the registration information of the sample already registered in the registration DB 108, the correction button 130 is pressed. When the correction button 130 is pressed, a screen (not shown) for selecting a sample registered in the registration DB 108 is displayed, and when a predetermined sample is selected, registration information on the selected sample is read out. , Is displayed on the sample information registration screen. In this case, the sample ID already assigned is displayed in the item of the sample ID 126.
  • the items of inspection 127 are buttons corresponding to each inspection belonging to the inspection result registration group, that is, food poisoning bacteria (toxin) button 132, radiation measurement button 133, virus inspection button 134, foreign matter contamination button 135, pesticide / antibiotics button 136 and an allergen mixing button 137 are displayed.
  • buttons 132 to 137 corresponding to the respective examinations belonging to the examination result registration group are pressed, a setting screen for setting details of examination contents of the respective examinations is displayed. Further, the buttons 132 to 137 of the item of the examination 127 are distinguished and displayed in different colors or the like in the case where the examination is already finished and the examination result is registered and the case where the examination is not performed. As a result, for the sample identified by the sample ID 126, it is possible to see at a glance which test of the items of the test 127 has been completed.
  • the items of survey 128 are buttons corresponding to each survey belonging to the survey result registration group, that is, health management (personal management) button 141, infection prevention measures (within facility) button 142, appearance, clothes, hairstyle, decoration button 143 And a hygiene education (knowledge) button 144 is displayed.
  • buttons 141 to 144 corresponding to each survey belonging to the survey result registration group are pressed, a setting screen for setting details of survey contents of each survey is displayed.
  • the buttons 141 to 144 of the items of the survey 128 are distinguished and displayed in different colors or the like depending on whether the survey has already been completed and the survey results have been registered and the survey has not been performed. As a result, for the sample identified by the sample ID 126, it is possible to know at a glance which of the items of the survey 128 has been completed.
  • the registration button 129 is pressed when registering (correcting) the input information in the registration DB 108 and returning to the main screen of FIG. 3.
  • the cancel button 131 is pressed to cancel the registration of information on the sample information registration screen and to return to the main screen of FIG.
  • FIG. 6 shows an example of the food poisoning bacteria test result registration screen.
  • each item of the sample ID 151 and the test count 152, a test result input field 153, and a registration button 154 and a cancel button 155 are displayed.
  • the sample ID of the sample for which the test result of the food poisoning bacteria test is registered is displayed.
  • the sample ID is specified by the user.
  • the number of examinations in the examination target period is displayed.
  • the inspection target period is described as one week.
  • "4 times" is displayed as the number of tests, and in this case, food poisoning bacteria tests are performed 4 times by changing the production date (lot) within one week specified in the test period. Will be implemented.
  • the number of examinations can be set on the setting screen displayed by pressing the food poisoning bacteria (toxin) button 132 on the sample information registration screen of FIG.
  • test items are 10 types of general living bacteria, coliform bacteria, mold, yeast, Staphylococcus aureus, cereus, Escherichia coli, salmonella, Vibrio parahaemolyticus, and thermostable bacteria.
  • the test items of the food poisoning bacteria test can be set on the setting screen displayed by pressing the food poisoning bacteria (toxin) button 132 of the sample information registration screen of FIG. There is no problem if the number of bacteria detected is 1 ⁇ 10 7 or less, and the other fungi are indicated as negative (-) or positive (+) if the number of bacteria detected is 1 ⁇ 10 7 or less. It is determined that there is no problem.
  • the registration button 154 is pressed to register (save) after inputting the test result of the food poisoning bacteria test.
  • the cancel button 155 is pressed to cancel the input of the test result of the food poisoning bacteria test and return to the main screen of FIG.
  • FIG. 7 shows an example of the pesticide / antibiotic test result registration screen.
  • a sample ID 161 In the agrochemical / antibiotic test result registration screen, a sample ID 161, a test result input field 162, a registration button 163, and a cancel button 164 are displayed.
  • the sample ID of the sample for registering the test result of the agrochemical / antibiotic test is displayed.
  • the sample ID is specified by the user.
  • test result input column 162 a result input column of the items of the agrochemical and the antibiotic which are set as the test target is displayed.
  • “1,1-dichloro-2,2-bis (4-ethylphenyl) ethane”, “1,2-dibromoethane”, “1-naphthaleneacetic acid”, “2- (10.01) 22 items of pesticides / antibiotics such as Naphthyl) Acetamide, "2, 2-DPA (Darapon)”, ... are set as test targets, and test results can be input. If a value equal to or greater than the reference value is detected, the value of the detection result is input, and if the detection result is undetected (undetectable level), “ND (NO DETECT)” is input.
  • the pesticide / antibiotic to be tested can be set on the setting screen displayed by pressing the pesticide / antibiotic button 136 on the sample information registration screen of FIG.
  • the pesticides / antibiotics that can be set as the test target are about 460 items shown in FIG. 8 to FIG.
  • FIG. 11 shows an example of a radiation measurement result registration screen.
  • the user presses the radiation measurement result registration button 73 on the main screen of FIG. 3. Thereby, the radiation measurement result registration screen of FIG. 11 is displayed.
  • each item of the sample ID 171 and the number of times of examination 172, a measurement result input field 173, a registration button 174 and a cancel button 175 are displayed.
  • the sample ID of the sample for which the measurement result of the radiation measurement is registered is displayed.
  • the sample ID is specified by the user.
  • the number of measurements in one week designated in the examination target period is displayed.
  • “three times” is displayed as the number of examinations, and in this case, radiation measurement is performed three times while changing the date within one week designated as the examination target period.
  • the number of examinations can be set on the setting screen displayed by pressing the radiation measurement button 133 on the sample information registration screen of FIG.
  • result input columns corresponding to the number of inspections displayed in the item of the number of inspections 172 are displayed.
  • the measurement items are cesium 137 and cesium 134. If the measured value is less than 10 BEC / kg, it is judged as normal (no problem), and if the measured value is 10 BEC / kg or more, it is judged as abnormal (NG) and input. In addition, you may determine whether it is normal by the sum total of the measured value of cesium 137 and cesium 134. As shown in FIG.
  • the registration button 174 is pressed to register (save) after the measurement result of the radiation measurement is input.
  • the cancel button 175 is pressed when canceling the input of the measurement result of the radiation measurement and returning to the main screen of FIG.
  • FIG. 12 shows an example of the foreign substance contamination inspection result registration screen.
  • the user presses the foreign substance contamination inspection result registration button 74 on the main screen of FIG. 3. Thereby, the foreign substance contamination inspection result registration screen of FIG. 12 is displayed.
  • each item of the sample ID 181 and the test frequency 182, the test result input column 183, the occurrence frequency input column 184, the comment input column 185, the comprehensive result display column 186, the registration button 187 and the cancel button 188 is displayed.
  • the sample ID of the sample for which the test result of the foreign substance contamination test is registered is displayed.
  • the sample ID is specified by the user.
  • the number of examinations 182 the number of examinations in one week designated in the examination target period is displayed.
  • “one” is displayed as the number of inspections, and in this case, one foreign substance contamination inspection is performed within one week designated in the inspection target period.
  • the number of inspections can be set on the setting screen displayed by pressing the foreign substance mixing button 135 on the sample information registration screen of FIG.
  • each inspection item of the foreign substance contamination inspection specifically, "X-ray detector”, “personal equipment”, “open air pollution”, “insect flying”, “anti-corrosion measures”, " The status of equipment deterioration, “cleaning frequency”, “presence of improvement team”, and “product storage state” are displayed.
  • This inspection item can also be set on the setting screen displayed by pressing the alien substance mixing button 135 on the sample information registration screen of FIG.
  • Each inspection item in the inspection result input column 183 is, for example, a toggle button, and the display of [OK] and [NG] is switched each time the inspection button is pressed. For each inspection item in the inspection result input field 183, either [OK] or [NG] is input.
  • the item “X-ray detector” is an inspection item for checking whether the facility is equipped with a metal detector for detecting foreign matter and can be used normally.
  • the item of "personal equipment” is an inspection item to check whether there is a provision for personal equipment.
  • the item “outside air pollution” is an inspection item for inspecting whether there is outside air pollution.
  • the item “Insect flying” is an inspection item for testing whether there is an insect flying countermeasure (insect countermeasure).
  • “Anti-corrosion measures” is an inspection item to check if there is a plagiarism measure.
  • the item of “Aging condition of equipment” is an inspection item for inspecting whether the maintenance of the equipment is in good condition.
  • the item “cleaning frequency” is an inspection item for inspecting whether there is a cleaning record.
  • the item of "presence of improvement team” is an inspection item which defines improvement team, such as improvement team, in-house (facility, business establishment) and checks whether or not the execution record is present.
  • the item of "product storage state” is an inspection item for checking whether the storage state of the product or the raw material is appropriate.
  • the occurrence frequency input field 184 the result of the user interviewing the worker with the occurrence frequency of the foreign matter contamination is input.
  • the occurrence frequency input field 184 is to select and enter any of daily occurrence, weekly occurrence, monthly occurrence, monthly occurrence, or no occurrence for more than half a year. ing.
  • the integrated result display column 186 integrated judgment results (OK, NG) based on each inspection item of the inspection result input column 183 are displayed. For example, when there is an item of [NG] even in one or more inspection items of the inspection result input column 183, the comprehensive determination result is determined as NG.
  • the registration button 187 is pressed when registering (saving) after the inspection result of the foreign substance contamination inspection is input.
  • the cancel button 188 is pressed to cancel the input of the inspection result of the foreign substance contamination inspection and to return to the main screen of FIG. 3.
  • FIG. 13 shows an example of the allergen contamination test result registration screen.
  • the user presses the allergen contamination test result registration button 75 on the main screen of FIG. 3. Thereby, the allergen contamination test result registration screen of FIG. 13 is displayed.
  • each item of the sample ID 191 and the test count 192, a test result input column 193, a registration button 194 and a cancel button 195 are displayed.
  • the sample ID of the sample for which the test result of the allergen contamination test is registered is displayed.
  • the sample ID is specified by the user.
  • the number of examinations in one week designated in the examination target period is displayed.
  • “three times” is displayed as the number of examinations, and in this case, three days of the allergen contamination examination are performed by changing the date within one week designated in the examination target period.
  • the number of examinations can be set on the setting screen displayed by pressing the allergen mixing button 137 on the sample information registration screen of FIG.
  • result input columns corresponding to the number of inspections displayed in the item of the number of inspections 192 are displayed.
  • the test items of the allergen contamination test are six items that are required to display buckwheat, wheat, peanuts, milk, eggs, and crustacea (shrimp, crab).
  • the inspection item can be set on the setting screen displayed by pressing the allergen mixing button 137 on the sample information registration screen of FIG. If an allergen contaminant is detected at 0.1 ppm or more, a positive (+) is input as a detection result, and if it is less than 0.1 ppm, a negative (-) is input. If all the detection results are negative (-), it is determined that there is no problem.
  • the registration button 194 is pressed to register (save) after inputting the test result of the allergen contamination test.
  • the cancel button 195 is pressed to cancel the input of the test result of the allergen contamination test and to return to the main screen of FIG. 3.
  • FIG. 14 shows an example of a virus test result registration screen.
  • the user presses the virus test result registration button 76 on the main screen of FIG. 3 when registering the test result of the norovirus test for the sample and the worker. Thereby, the virus test result registration screen of FIG. 14 is displayed.
  • each item of the sample ID 201 and the test count 202, a test result input field 203, a registration button 204 and a cancel button 205 are displayed.
  • the sample ID of the sample for which the test result of the virus test is registered is displayed.
  • the sample ID is specified by the user.
  • the total number of examinations in one week designated in the examination target period is displayed.
  • “nine times” is displayed as the number of examinations, and the manufacturing date (lot) is changed within one week designated as the examination target period, and three times for each of three workers and the sample.
  • a total of nine test results are input by performing the virus test of.
  • the number of workers to be inspected, the number of products, and the number of inspections per person (one) can be set on the setting screen displayed by pressing the virus inspection button 134 of the sample information registration screen of FIG.
  • inspection result input column 203 result input columns corresponding to the number of inspections displayed in the item of the number of inspections 202 are displayed.
  • test result when norovirus is detected, positive (+) is input, and negative (-) is input if it is not detected. If all test results are negative (-), it is determined that there is no problem.
  • the registration button 204 is pressed to register (save) after the inspection result of the virus inspection is input.
  • the cancel button 205 is pressed to cancel the input of the inspection result of the virus inspection and to return to the main screen of FIG.
  • FIG. 15 shows an example of a health management survey result registration screen.
  • each item of sample ID 211 and survey number of people 212, survey subject switch button 213, survey subject input column 214, survey result input column 215, registration button 216 and cancel button 217 are displayed Be done.
  • the sample ID of the sample for which the survey result of the health management survey is registered is displayed.
  • the sample ID is specified by the user.
  • the number of persons who carry out the health management survey within one week designated in the examination target period is displayed.
  • “five people” are displayed as the number of persons in the survey, and in this case, a health management survey is conducted on five workers within one week designated as the examination target period.
  • the survey number can be set on the setting screen displayed by pressing the health management (personal management) button 141 of the sample information registration screen of FIG.
  • the survey target person switching button 213 is pressed when the display of the survey target person input field 214 and the survey result input field 215 held for each survey target person is switched.
  • a survey target person input column 214 and a survey result input column 215 for the “second person” survey target are displayed.
  • attribute information of the survey target person is input.
  • the attribute information is, for example, company name, department, name, gender and the like.
  • the survey result input field 215 displays each survey item on health management to be managed by an individual.
  • survey items such as “having diarrhea”, “having a cold, having a cold”, “having an injury”, “having rough hands or rough skin”, etc. Is displayed.
  • Each survey item of health management to be managed by an individual can be set on the setting screen displayed by pressing the health management (personal management) button 141 of the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 215.
  • FIG. 15 shows an example of one survey result for the second of five survey subjects, if a check is input even for one of the survey items, the survey result for that time is It is judged to be unsuitable.
  • the registration button 216 is pressed when registering (saving) after entering the survey result on health management.
  • the cancel button 217 is pressed to cancel the input of the research result on health management and return to the main screen of FIG. 3.
  • FIG. 16 shows an example of the infection prevention countermeasure research result registration screen.
  • the user presses the infection prevention measures research result registration button 82 on the main screen of FIG. 3. Thereby, the infection prevention countermeasure research result registration screen of FIG. 16 is displayed.
  • the sample ID of the sample for which the investigation result of the infection prevention countermeasure investigation is registered is displayed.
  • the sample ID is specified by the user.
  • the number of persons who carry out the infection prevention countermeasure investigation within one week designated in the inspection target period is displayed.
  • “five people” are displayed as the number of persons in the investigation, and in this case, an infection prevention countermeasure investigation is carried out for five workers within one week designated in the inspection target period.
  • the number of survey persons can be set on the setting screen displayed by pressing the infection prevention countermeasure (within facility) button 142 of the sample information registration screen of FIG. 5.
  • the survey target person switching button 223 is pressed when the display of the survey target person input column 224 and the survey result input column 225 held for each survey target person is switched.
  • a survey target person input column 224 and a survey result input column 225 for the “second person” survey target are displayed.
  • attribute information of the survey subject is input.
  • the attribute information is, for example, company name, department, name, gender and the like.
  • each survey item regarding infection prevention measures of the facility is displayed.
  • “handwashing equipment is not appropriate” “contaminated area / non-contaminated area is not divided”, “work flow line is mixed”, “no record of receipt of material received”, ⁇ ⁇ ⁇ ⁇ Investigation items such as are displayed.
  • Each survey item of the infection prevention measures can be set on the setting screen displayed by pressing the infection prevention measures (within facility) button 142 of the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 225.
  • FIG. 16 shows an example of the result of one survey for the second person out of five survey subjects, but if one of the survey items has a check input, the survey results for that time are It is judged to be unsuitable.
  • the registration button 226 is pressed when registering (storing) after entering the investigation result on the infection prevention measures.
  • the cancel button 227 is pressed to cancel the input of the investigation result on the infection prevention measures and to return to the main screen of FIG. 3.
  • FIG. 17 shows an example of the appearance, clothes, hair style and decoration research result registration screen.
  • the user presses the appearance, clothes, hair style and decoration research result registration button 83 on the main screen of FIG. As a result, the appearance, clothes, hair style and decoration research result registration screen of FIG. 17 is displayed.
  • each item of the sample ID 231 and the number of survey persons 232, a survey subject switch button 233, a survey subject input column 234, a survey result input column 235, a registration button 236 and A cancel button 237 is displayed.
  • the sample ID of the sample for registering the result of the survey on appearance, clothes, hair style and decoration is displayed.
  • the sample ID is specified by the user.
  • the number of persons who carry out a survey on their appearance, clothes, hairstyles and decorations within one week designated in the examination target period is displayed.
  • “5” is displayed as the number of persons surveyed, and in this case, surveys of appearance, clothes, hairstyles, and decorations for 5 workers are performed within one week designated as the inspection period.
  • the number of persons to be surveyed can be set on the setting screen displayed by pressing the appearance / dress / hair style / decoration button 143 of the sample information registration screen of FIG. 5.
  • the survey target person switching button 233 is pressed when the display of the survey target person input column 234 and the survey result input column 235 held for each survey target person is switched.
  • a survey target person input column 234 and a survey result input column 235 for the “second” survey target person are displayed.
  • attribute information of the survey target person is input.
  • the attribute information is, for example, company name, department, name, gender and the like.
  • the survey result input field 235 displays each survey item on the appearance, clothes, hair style and decoration.
  • Survey items are displayed.
  • the individual survey items of the appearance, clothes, hair style and decoration investigation can be set on the setting screen displayed by pressing the appearance, clothes, hair style and decoration button 143 of the sample information registration screen of FIG.
  • the user inputs a check in the corresponding item of the survey result input field 235.
  • FIG. 17 shows an example of one survey result for the second person among the five survey subjects, but if even one of the survey items has a check input, the survey result for that time is It is judged to be unsuitable.
  • the registration button 236 is pressed in the case of registration (storage) after the search results on the appearance, clothes, hairstyle and decoration are input.
  • the cancel button 237 is pressed to cancel the input of the research result on the appearance, clothes, hairstyle and decoration and to return to the main screen of FIG.
  • FIG. 18 shows an example of the hygiene education research result registration screen.
  • each item of sample ID 241 and survey number of people 242, survey target person switching button 243, survey target person input column 244, survey result input column 245, registration button 246 and cancel button 247 are displayed Be done.
  • the sample ID of the sample for which the survey result on the hygiene education is registered is displayed.
  • the sample ID is specified by the user.
  • the number of persons who conduct surveys on hygiene education within one week designated as the inspection target period is displayed.
  • "5" is displayed as the number of surveys, and in this case, a survey on hygiene education is conducted for 5 workers within one week specified in the inspection period.
  • the number of persons surveyed can be set on the setting screen displayed by pressing the hygiene education (knowledge) button 144 of the sample information registration screen of FIG. 5.
  • the survey target person switching button 243 is pressed when the display of the survey target person input field 244 and the survey result input field 245 held for each survey target person is switched.
  • a survey target person input column 244 and a survey result input column 245 for the “second” survey target person are displayed.
  • attribute information of the survey subject is input.
  • the attribute information is, for example, company name, department, name, gender and the like.
  • each survey item related to hygiene education is displayed.
  • “monthly stool examination is not performed (frequency)” “all stool examinations are not performed (subject)”, “we do not know fear of food poisoning bacteria”, Survey items such as "I do not know how to wash my hands” are displayed.
  • Each survey item on hygiene education can be set on the setting screen displayed by pressing the hygiene education (knowledge) button 144 on the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 245.
  • FIG. 18 shows an example of the result of one survey for the second person among the five survey subjects, but if one of the survey items has a check input, the survey results for that time are It is judged to be unsuitable.
  • the registration button 246 is pressed in the case of registration (storage) after inputting the survey result on hygiene education.
  • a cancel button 247 is pressed to cancel the input of the survey result on hygiene education and return to the main screen of FIG. 3.
  • FIG. 19 shows an example of the result list screen.
  • each item of customer name 251, facility name 252, facility CD 253, sub CD 254, sample name 255, sample ID 256, test result display column 257, survey date 258, and surveyor 259, and close button 260 are displayed. Be done.
  • the customer name 251, the facility name 252, the facility CD 253, and the sub CD 254 in the result list screen include the customer name 121, the facility name 122, the facility CD 123, and the sub CD 124 of the sample information registration screen.
  • the name and facility name and its code number (CD) are displayed.
  • search buttons 251A and 252A are added to the customer name 251 and the facility name 252, respectively.
  • the customer name 251 the company name of the customer selected from the customer list displayed by the user pressing the search button 251A is displayed.
  • the facility name 252 the facility name selected from the facility name list displayed by the user pressing the search button 252A is displayed.
  • sample name 255 and the sample ID 256 similarly to the sample name 125 and the sample ID 126 on the sample information registration screen, the name of the inspected food and the sample ID are displayed.
  • Search buttons 255A and 256A are added to the sample name 255 and the sample ID 256, respectively.
  • As the sample name 255 a product name selected from the sample list displayed by pressing the search button 255A is displayed.
  • the sample ID 256 the sample ID selected from the sample ID list displayed by pressing the search button 256A is displayed.
  • test results are displayed for the sample identified by the sample ID displayed in the sample ID 256 within the range in which the test has been completed.
  • the non-displayed test results can be displayed by scrolling.
  • the date on which the examination and investigation were performed on the sample identified by the sample ID displayed in the sample ID 256 is displayed.
  • the last (last) date is displayed.
  • the names of persons in charge who have investigated the sample identified by the sample ID displayed in the sample ID 256 are displayed.
  • the close button 260 is pressed when ending the display of the result list screen and returning to the main screen of FIG. 3.
  • FIG. 20 shows an example of the result output screen.
  • each item of the customer name 271, the facility name 272, the facility CD 273, the sub CD 274, the sample name 275, the sample ID 276, and the scale determination result display field 277, the close button 278 and the certificate issuance button 279 are displayed. Ru.
  • the customer name 271, the facility name 272, the facility CD 273, the sub CD 274, the sample name 275, and the sample ID 276 are the customer name 251, the facility name 252, the facility CD 253, the sub CD 254, the sample name 255, and the sample of the result list screen in FIG. The same as ID 256, respectively.
  • Search buttons 271A, 272A, 275A, and 276A are also added to the customer name 271, the facility name 272, the sample name 275, and the sample ID 276, respectively.
  • the safety degree for the health damage calculated by the safety degree calculation unit 106 is determined based on the examination result and the examination result for the sample identified by the sample ID displayed in the sample ID 256 Displayed as a result.
  • the degree of safety displayed in the scale determination result display field 277 is represented by a value in the exponential format.
  • the safety degree calculated by the safety degree calculation unit 106 includes a color assigned according to the magnitude of the safety degree.
  • the calculation method of the safety degree by the safety degree calculation unit 106 will be described later. The user can grasp the degree of safety of the sample at a glance by the value "-9" of the exponent part of the degree of safety expressed by a power of 10 and the color corresponding to the degree of safety.
  • the safety degree color sample scale 277A is represented by the shade from black to white according to the magnitude of the safety degree, but on a screen where color display is possible, For example, according to the degree of safety, a color corresponding to the wavelength of visible light is assigned and displayed such that a cold color system in the vicinity of 10 -2 becomes a warm color system in the vicinity of 10 -2 and a red color around 10 -10. ing.
  • the close button 278 is pressed when ending the display of the result output screen and returning to the main screen of FIG. 3.
  • the certificate issuance button 279 is pressed when issuing a test certificate of the degree of safety of the sample.
  • an inspection certificate as shown in FIG. 21 is printed.
  • the value “-9” of the index portion of the safety degree of the sample calculated by the safety degree calculation unit 106 is displayed in a large size, and the gray color (color color corresponding to the safety degree The mark (star) is attached using).
  • the value “ ⁇ 9” and the gray color of the exponent part of the degree of safety of the sample displayed here are the same as the value of the degree of safety and the gray color displayed in the result display portion 277B of FIG.
  • the magnitude of the risk (the degree of risk) of the sample is calculated based on the examination result and the examination result of the sample input by the user from the main screen. And, it is defined that the safety level of the sample for the health hazard is given by the reciprocal of the calculated magnitude of the risk, considering that it is the reverse of the magnitude of the calculated risk (risk level).
  • the risk influence degree is determined by the risk influence degree determination unit 104, for example, in n (n> 1) stages. For example, if it is judged that the degree of influence of risk is in five stages, "5: level directly linked to human death, 4: possible human death, 3: crisis at representative level, 2: slightly affected, 1: In accordance with the standard that “there is almost no effect”, the degree of risk influence of each inspection / study item is preset as shown in FIG.
  • the degree of risk of food poisoning bacteria is a serious problem if even one toxin is detected, as shown in FIG. If no one is detected, the degree of influence is set to "1".
  • the frequency of risk of food poisoning bacteria is set to the same value as the risk impact. That is, the occurrence frequency is set to "5" when at least one toxin is detected, and the occurrence frequency "1" when no toxin is detected.
  • the frequency of occurrence of risks for pesticides and antibiotics is set to the same value as the risk impact.
  • a value equal to or higher than the reference value is detected for “4-chlorophenoxyacetic acid (4-CPA)”.
  • the risk impact determination unit 104 determines that the risk impact is “5”
  • the occurrence frequency of risk of radiation measurement is set to “1” which is the minimum value in the case of all undetected (less than the reference value), and the number of times of detection is set in the case of one or more detections.
  • the risk influence degree determination unit 104 determines the degree of influence of the risk as “1” because the detection result is not detected in all the three examinations.
  • the influence level of the risk of foreign body contamination is “5: when the level occurs daily, 4: when the level occurs weekly, 3: when the level occurs monthly, 2: several months If it is a level that occurs once, it is set as “1: when it has not occurred for more than half a year”.
  • the frequency of occurrence of the risk of contamination is “X-ray detector”, “personal equipment”, “open air pollution”, “insect flying”, “anti-corrosion measures”, “equipment condition”, “cleaning frequency”, “ The number of inspection items determined as “NG” is set among the inspection items “presence of improvement team” and “product storage state”.
  • the occurrence frequency of the risk of mixing with the allergen is set to “1” which is the minimum value if not all detected, and the number of times of detection is set if detected once or more.
  • the degree of influence of the risk of virus testing is a serious problem if even one toxin is detected, the degree of influence “5” if one toxin is detected, one If one is not detected, the degree of influence is set to "1".
  • the occurrence frequency of the risk of virus inspection is set to “1” which is the minimum value if not all detected, and the number of times of detection is set if detected once or more.
  • the risk influence determination unit 104 determines that the risk influence degree
  • the impact of health management risk is as follows: “5: If there are 5 unfit people, 4: If there are 4 unfit people, 3: If there are 3 unfit people, 2: If there are 2 unfit people, 1: It is set as "when the unsuitable person is 1 or less".
  • the frequency of health care risk occurrence is set to the sum of the number of surveys judged to be unsuitable.
  • the impact of the infection prevention measures is "5: If there are 5 unfit people, 4: If there are 4 unfit people, 3: If there are 3 unfit people, 2: If there are 2 unfit people , 1: when the unsuitable person is 1 or less. "
  • the frequency of risk of infection control measures is set to the total number of surveys judged to be unsuitable.
  • the example of the infection prevention measures survey result registration screen in FIG. 16 is one survey result for the second of five survey subjects, but for two of the five survey subjects, It is assumed that the survey results determined to be unsuitable are registered one by one.
  • the frequency of the risk of appearance, clothes, hairstyle and decoration is set to the sum of the number of surveys judged to be unsuitable.
  • the example of the appearance / dress / haircut / decoration research result registration screen shown in FIG. 17 is one survey result for the second of five persons to be surveyed, but one of five persons to be surveyed
  • the survey result judged to be unsuitable is registered only once.
  • the influence level of the risk of hygiene education is "5: When there are 5 unfit people, 4: When there are 4 unfit people, 3: When there are 3 unfit people, 2: When there are 2 unfit people, 1: It is set as "when the unsuitable person is 1 or less”.
  • the risk occurrence frequency of hygiene education is set to the sum of the number of surveys judged to be unsuitable.
  • the magnitude of the risk calculated for each inspection item and investigation item is as follows.
  • the risk of food poisoning bacteria (toxins) 5 ⁇ 5 25
  • the magnitude of the risk of pesticides and antibiotics 5 ⁇ 5 25
  • Risk of contamination 5 x 4 20
  • the risk of allergen contamination 5 ⁇ 2 10
  • the magnitude of the risk of virus testing 5 ⁇ 3 15
  • Health management risk magnitude 3 ⁇ 3 9
  • Risk of infection prevention measures 2 ⁇ 2 4
  • the size of the risk of appearance, clothes, hairstyle and decoration 1 ⁇ 1 1
  • the magnitude of the risk of hygiene education 2 ⁇ 2 4
  • the risk influence degree determination unit 104 determines the degree of influence of the risk of the sample on the basis of the examination result and the examination result registered in the examination result registration group and the examination result registration group. 105 determines the occurrence frequency of the risk of the sample based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Then, the safety degree calculation unit 106 calculates the magnitude of the risk using the calculated risk impact degree of each item and the frequency of occurrence of the risk, and the magnitude of the calculated risk indicates that the health damage Calculate the degree of safety.
  • the determination method of the influence degree of the risk of each item mentioned above, and the determination method of the occurrence frequency of risk are an example until it gets tired, and it is not limited to this.
  • step S1 the test result registration unit 102 acquires the result of each test item belonging to the test result registration group of the sample to be calculated. Specifically, the test results of the food poisoning bacteria test of the sample inputted by the food poisoning bacteria test result registration screen of FIG. 6, and the contents of the pesticides / antibiotics of the sample inputted by the pesticides / antibiotics test result registration screen of FIG. Test result of amount, test result of radiation dose of sample inputted by radiation measurement result registration screen of FIG. 11, test result of allergen contamination test of sample inputted by foreign matter contamination test result registration screen of FIG. 12, and The test result of the norovirus test for the specimen and the worker input by the 14 virus test result registration screens is acquired.
  • step S2 the survey result registration unit 103 acquires the result of each survey item belonging to the survey result registration group of the sample to be calculated. Specifically, for the sample to be calculated, the infection prevention measures of the facility input by the health management survey result registration screen of FIG. 15 and the health management survey result input by the health management survey result registration screen of FIG. Survey results on the appearance, clothes, hairstyle, decoration of the worker entered by the appearance, clothes, hairstyle, decoration research results registration screen of FIG. 17 and the hygiene education research results registration screen of FIG. 18 The survey results on the health education system and the understanding level of workers are obtained.
  • step S3 the risk influence degree determination unit 104 determines the degree of risk influence degree for each inspection result or investigation result based on the inspection result and the investigation result acquired in step S1 and step S2.
  • step S4 the risk occurrence frequency determination unit 105 determines the occurrence frequency of risk for each test result or check result based on the check result and the check result acquired in step S1 and step S2.
  • step S5 the safety degree calculation unit 106 calculates the magnitude of the risk for each examination item belonging to the examination result registration group or the examination item belonging to the investigation result registration group.
  • the magnitude of the risk of each test item or each survey item is calculated by the product of the impact of the risk and the frequency of occurrence of the risk.
  • step S6 the safety degree calculation unit 106 calculates the magnitude of the risk of the sample using the calculated magnitudes of the risks of all the test items and the survey items.
  • the magnitude of the risk of the sample is calculated by the product of the magnitude of the risk of all test items and survey items.
  • step S7 the safety degree calculation unit 106 calculates the degree of safety of the sample using the calculated magnitude of the risk of the sample.
  • the degree of safety of the sample is calculated by the reciprocal of the calculated magnitude of risk.
  • the calculated degree of safety of the sample is stored in the registration DB 108, and is read out as necessary, for example, when the result list button 91 or the result output button 92 is pressed on the main screen of FIG.
  • the safety scale system 1 to which the present invention is applied is to define, judge and evaluate the safety (safety) of human health damage based on the new standard.
  • Safety Level Scale System 1 the safety level against human health damage is the inverse of the calculated risk size, considering that the safety level against human health damage is the reverse of the magnitude of risk (risk level).
  • the color color of the visible light wavelength corresponding to the calculated degree of safety is displayed, for example, on the label or package of the sample (food), so that the general consumer can display the degree of safety displayed on the label or package, etc. By just looking at the color that indicates, you can grasp the degree of safety of the food.
  • the value of the calculated degree of safety or the color color corresponding thereto can be used as an absolute index indicating the degree of security or a relative index. That is, according to the safety degree scale system 1, it is possible to provide an index that can comprehensively judge the safety degree against health damage.
  • the safety degree scale system 1 inspects and evaluates the degree of safety of food manufactured in elementary or junior high schools, factories, offices, kitchens or cafeterias such as nursing homes, shops of restaurants, food factories etc.
  • safety scale system 1 can be applied to distribution processes and production processes of agricultural products and feeds as well as establishments dealing with products (foods) eaten by humans. It can also be used as a system to inspect and evaluate the degree of safety (reliability) against the health damage of animals.
  • a system means a set of a plurality of components (apparatus, modules (parts), etc.), and it does not matter whether all the components are in the same case. Therefore, a plurality of devices housed in separate housings and connected via a network, and one device housing a plurality of modules in one housing are all systems. .
  • the present invention can have a cloud computing configuration in which one function is shared and processed by a plurality of devices via a network.
  • each step described in the above-described flowchart can be executed by one device or in a shared manner by a plurality of devices.
  • the plurality of processes included in one step can be executed by being shared by a plurality of devices in addition to being executed by one device.

Abstract

The present invention relates to an information processing device, method, and program, whereby it is possible to provide an index allowing comprehensive determination of safety with respect to harm to health. An impact determination unit determines an impact of a risk with respect to harm to health. A frequency determination unit determines a frequency of occurrence of the risk. A safety computation unit uses the determined impact of the risk and the determined frequency of occurrence of the risk to compute the magnitude of the risk, and computes safety with respect to harm to health from the computed size of the risk. It would be possible to apply the present invention, as an example, to an information processing device, etc., which computes safety with respect to harm to health.

Description

情報処理装置および方法、並びにプログラムINFORMATION PROCESSING APPARATUS AND METHOD, AND PROGRAM
 本発明は、情報処理装置および方法、並びにプログラムに関し、特に、健康被害に対する安全度を総合的に判断可能な指標を提供することができるようにする情報処理装置および方法、並びにプログラムに関する。 The present invention relates to an information processing apparatus and method, and a program, and more particularly to an information processing apparatus and method, and a program capable of providing an index that can comprehensively determine the degree of safety against health damage.
 近年、飲食店の店舗や、事業所などの食堂、食品工場等における衛生管理の強化が求められている。 In recent years, it has been required to strengthen hygiene management in restaurants, cafeterias such as business establishments, food factories and the like.
 これに対し、本出願人は、飲食店の店舗において食中毒を防止するため、店舗および従業員の衛生管理の状態、細菌に関する情報、並びに、顧客の視点からの衛生管理の状態それぞれについてスコア化し、総合評価することが可能な衛生管理システムを先に提案している(特許文献1参照)。 On the other hand, in order to prevent food poisoning at the restaurant, the applicant scores each of the condition of hygiene control of the store and the employee, information on bacteria, and the condition of hygiene control from the viewpoint of the customer. A hygiene management system that can be comprehensively evaluated has been proposed earlier (see Patent Document 1).
 また、東日本大震災による原子力発電所事故が発生して以来、環境中の放射線に対する不安が高まっており、農産物に含まれる放射線量にも関心が高まっている。 In addition, since the occurrence of a nuclear power plant accident caused by the Great East Japan Earthquake, concern about radiation in the environment has increased, and interest in radiation doses contained in agricultural products has also increased.
特開2010-287166号Unexamined-Japanese-Patent No. 2010-287166
 従来より、飲食店の店舗や事業所などの施設や従事者に対する衛生度、および、農産物などの食材や、それらを用いて加工・製造される食品に対して、細菌や添加物、放射線量などについて個別の基準値は存在する。 In the past, hygiene levels for facilities and workers such as restaurants and establishments, food materials such as agricultural products, and foods, processed and manufactured using them, bacteria, additives, radiation dose, etc. There are individual reference values for.
 しかしながら、上述のような様々な健康被害のリスクに対して、安全度(安心度)を総合的に判断するような指標がなかった。 However, there is no index that comprehensively determines the degree of safety (reliability) with respect to the risk of various health hazards as described above.
 本発明は、このような状況に鑑みてなされたものであり、健康被害に対する安全度を総合的に判断可能な指標を提供することができるようにするものである。 The present invention has been made in view of such a situation, and is intended to be able to provide an index that can comprehensively determine the degree of safety against health damage.
 本発明の一側面の情報処理装置は、
 健康被害に対するリスクの影響度を判定する影響度判定部と、
 前記リスクの発生頻度を判定する頻度判定部と、
 判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する安全度算出部と
 を備える。
An information processing apparatus according to one aspect of the present invention is
An impact determination unit that determines the impact of risk on health damage;
A frequency determination unit that determines the frequency of occurrence of the risk;
The degree of safety is calculated by calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk It has a department and
 本発明の一側面の情報処理方法は、
 健康被害に対するリスクの影響度を判定し、
 前記リスクの発生頻度を判定し、
 判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する
 ステップを含む。
An information processing method according to one aspect of the present invention is
Determine the impact of risk on health hazards,
Determine the frequency of occurrence of the risk,
Calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk .
 本発明の一側面のプログラムは、
 コンピュータに、
 健康被害に対するリスクの影響度を判定し、
 前記リスクの発生頻度を判定し、
 判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する
 処理を実行させる。
The program according to one aspect of the present invention is
On the computer
Determine the impact of risk on health hazards,
Determine the frequency of occurrence of the risk,
The magnitude of the risk is calculated using the determined degree of influence of the risk and the frequency of occurrence of the risk, and the process of calculating the degree of safety against health damage from the magnitude of the calculated risk is performed. Let
 本発明の一側面においては、健康被害に対するリスクの影響度が判定され、前記リスクの発生頻度が判定され、判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさが算出され、算出された前記リスクの大きさから、健康被害に対する安全度が算出される。 In one aspect of the present invention, the degree of risk impact on health damage is determined, the frequency of occurrence of the risk is determined, and the degree of impact of the risk determined and the frequency of occurrence of the risk are used to determine the risk. The degree of safety against health damage is calculated from the calculated magnitude of the risk.
 本発明の一側面によれば、健康被害に対する安全度を総合的に判断可能な指標を提供することができる。 According to one aspect of the present invention, it is possible to provide an index that can comprehensively determine the degree of safety against health damage.
本発明を適用した安全度スケールシステムの構成例を示すブロック図である。It is a block diagram showing an example of composition of a safety degree scale system to which the present invention is applied. サーバのハードウェア構成例を示すブロック図である。It is a block diagram showing the example of hardware constitutions of a server. メイン画面の例を示す図である。It is a figure which shows the example of a main screen. 安全度スケールシステムの機能的構成例を示すブロック図である。It is a block diagram showing an example of functional composition of a degree-of-safety scale system. サンプル情報登録画面の例を示す図である。It is a figure which shows the example of a sample information registration screen. 食中毒細菌検査結果登録画面の例を示す図である。It is a figure which shows the example of a food poisoning bacteria test-result registration screen. 農薬・抗生物質検査結果登録画面の例を示す図である。It is a figure which shows the example of an agrochemical * antibiotic test result registration screen. 農薬・抗生物質の例を示す図である。It is a figure which shows the example of agrochemical and an antibiotic. 農薬・抗生物質の例を示す図である。It is a figure which shows the example of agrochemical and an antibiotic. 農薬・抗生物質の例を示す図である。It is a figure which shows the example of agrochemical and an antibiotic. 放射線測定結果登録画面の例を示す図である。It is a figure which shows the example of a radiation measurement result registration screen. 異物混入検査結果登録画面の例を示す図である。It is a figure which shows the example of a foreign material contamination test result registration screen. アレルゲン混入検査結果登録画面の例を示す図である。It is a figure which shows the example of an allergen mixing test result registration screen. ウイルス検査結果登録画面の例を示す図である。It is a figure which shows the example of a virus test result registration screen. 健康管理調査結果登録画面の例を示す図である。It is a figure which shows the example of a health-care research result registration screen. 感染予防対策調査結果登録画面の例を示す図である。It is a figure which shows the example of the infection prevention countermeasure investigation result registration screen. 身なり・服装・髪型・装飾調査結果登録画面の例を示す図である。It is a figure which shows the example of appearance, clothes, a hair style, and decoration research result registration screen. 衛生教育調査結果登録画面の例を示す図である。It is a figure which shows the example of a hygiene education research result registration screen. 結果一覧画面の例を示す図である。It is a figure which shows the example of a result list screen. 結果出力画面の例を示す図である。It is a figure which shows the example of a result output screen. 検査証明書の例を示す図である。It is a figure which shows the example of a test | inspection certificate. リスクの影響度の設定例を示す図である。It is a figure which shows the example of a setting of the influence degree of risk. 安全度算出処理を説明するフローチャートである。It is a flowchart explaining safety degree calculation processing.
<安全度スケールシステムの構成例>
 図1は、本発明を適用した安全度スケールシステムの構成例を示すブロック図である。
<Example of configuration of safety scale system>
FIG. 1 is a block diagram showing a configuration example of a safety degree scale system to which the present invention is applied.
 図1の安全度スケールシステム1は、例えば、食中毒、放射線、衛生管理、微生物、などの、人間の健康被害に対する安全度(安心度)を検査・評価するシステムである。 The safety scale system 1 of FIG. 1 is a system that inspects and evaluates safety (safety) of human health damage such as food poisoning, radiation, hygiene management, microbes, and the like.
 安全度スケールシステム1は、例えば、小中学校、工場、オフィス、介護施設などの厨房または食堂、飲食店の店舗、食品工場などの事業所で利用され、各事業所で製造される食品の安全度を検査・評価し、出力する。 The safety scale system 1 is used, for example, in elementary or junior high school, a factory, an office, a kitchen or cafeteria such as a nursing home, a restaurant store, a food factory, etc. Examine, evaluate and output.
 安全度スケールシステム1は、多数の事業所の衛生状態を一元的に管理することができ、特に、全国や一定の地域に多数(複数)の事業所などを展開している場合に有用なシステムである。本実施の形態では、飲食店のチェーン展開をしている会社のチェーン店において、各店舗で製造されて提供される商品(食品)の安全度を検査する例について説明する。 The safety scale system 1 can centrally manage the hygiene status of many business sites, and is particularly useful when many business sites are deployed throughout the country or certain regions. It is. In the present embodiment, an example will be described in which the degree of safety of a product (food) manufactured and provided at each store is inspected at a chain store of a company that is expanding a restaurant chain.
 従って、図1の安全度スケールシステム1は、換言すれば、飲食店のチェーン展開をしている会社のチェーン店の複数の店舗で提供される商品の安全度を一元的に管理する。 Therefore, in other words, the safety scale system 1 of FIG. 1 centrally manages the safety of products provided at a plurality of stores of a chain store of a company that is expanding a restaurant chain.
 安全度スケールシステム1は、サーバ11と1以上の端末装置12とで構成される。図1では、3台の端末装置12-1乃至12-3が図示されているが、端末装置12の個数は、必要に応じて増減させることができる。サーバ11と端末装置12とは、インターネット、LAN(Local Area Network)、VPN(Virtual Private Network)などのネットワークにより接続されている。 The security level scale system 1 is configured of a server 11 and one or more terminal devices 12. Although three terminal devices 12-1 to 12-3 are illustrated in FIG. 1, the number of terminal devices 12 can be increased or decreased as needed. The server 11 and the terminal device 12 are connected by a network such as the Internet, a LAN (Local Area Network), or a VPN (Virtual Private Network).
 安全度検査を行うための情報を処理する情報処理装置としてのサーバ11は、安全度検査を行うためのアプリケーションプログラム(以下、安全度検査プログラムという。)を実行する。 The server 11 as an information processing apparatus that processes information for performing a safety degree inspection executes an application program (hereinafter, referred to as a safety degree inspection program) for performing a safety degree inspection.
 端末装置12は、例えば、パーソナルコンピュータ(ノート型を含む)、タブレット端末、いわゆるスマートフォンと呼ばれる高機能携帯電話機、専用の入力端末などである。端末装置12は、各店舗に据え置かれていたり、あるいは、各店舗を巡回し、店舗の衛生状態等を調査する調査員により携行されている。 The terminal device 12 is, for example, a personal computer (including a notebook type), a tablet terminal, a high-performance mobile phone called a so-called smartphone, a dedicated input terminal, or the like. The terminal device 12 is kept at each store or is carried by an investigator who patrols each store and investigates the hygiene condition and the like of the store.
 各店舗の店長などの店舗責任者、店舗を運営する会社の衛生状態を管理する管理責任者、または、調査員等(以下、総称してユーザという。)が端末装置12を操作し、端末装置12は、安全度検査プログラムが実行されているサーバ11にアクセスする。 A store manager such as a store manager of each store, a manager responsible for managing the sanitary condition of the company operating the store, or an investigator (hereinafter collectively referred to as a user) operates the terminal device 12 to operate the terminal device 12 accesses the server 11 on which the safety check program is executed.
 サーバ11により実行される安全度検査プログラムは、例えば、HTML等のマークアップ言語により作成されたWEBアプリケーションであり、安全度検査プログラムにより作成された所定の画面が、端末装置12上で実行されるブラウザによって端末装置12のディスプレイに表示される。ブラウザは、例えば、HTML(Hypertext Markup Language)文書を解釈し、ディスプレイなどに画面を表示する表示機能や、URL(Uniform Resource Locators)を設定することにより、サーバ11のWEBサイトにアクセスさせ、データをダウンロードしたり、あるいはサイトにデータを送信したりする通信機能や、あるいはHTML文書中でリンクが張られたURLにジャンプするジャンプ機能などの基本的な機能を備えている。 The security level inspection program executed by the server 11 is, for example, a WEB application created in a markup language such as HTML, and a predetermined screen created by the security level inspection program is executed on the terminal device 12 It is displayed on the display of the terminal device 12 by the browser. The browser, for example, interprets an HTML (Hypertext Markup Language) document and displays a screen on a display or the like, or sets a URL (Uniform Resource Locators) to access the web site of the server 11 and access the data. It has basic functions such as a communication function that downloads or sends data to a site, or a jump function that jumps to a linked URL in an HTML document.
 端末装置12は、安全度検査プログラムによりディスプレイに表示される所定の画面に対してユーザが行う操作(入力)を受け付け、操作された内容をネットワークを介してサーバ11に送信する。 The terminal device 12 receives an operation (input) performed by the user on a predetermined screen displayed on the display by the safety level inspection program, and transmits the operated content to the server 11 via the network.
 安全度検査プログラムが実行されているサーバ11は、端末装置12で操作された内容を受信し、操作された内容に応じて、予め決められたデータ処理を行ったり、次の画面を端末装置12に表示させたりする。 The server 11 on which the safety level inspection program is executed receives the content operated by the terminal device 12 and performs predetermined data processing according to the content operated, or the next screen is displayed on the terminal device 12. Or display it.
<サーバ11のハードウェア構成例>
 図2は、サーバ11のハードウェア構成例を示している。
<Hardware Configuration Example of Server 11>
FIG. 2 shows an example of the hardware configuration of the server 11.
 図2のサーバ11において、CPU(Central Processing Unit)31は、ROM(Read Only Memory)32、または記憶部38に記憶されているプログラムにしたがって各種の処理を実行する。ここでいうプログラムには、上述した安全度検査プログラムは勿論、例えば、ウィンドウズ(登録商標)などのOS(Operating System)やネットワークアダプタのドライバ等も含まれる。RAM(Random Access Memory)33には、CPU31が実行するプログラムやデータなどが適宜記憶される。これらのCPU31、ROM32、およびRAM33は、バス34により相互に接続されている。 In the server 11 of FIG. 2, a central processing unit (CPU) 31 executes various processes in accordance with a program stored in a read only memory (ROM) 32 or a storage unit 38. The program mentioned here includes, for example, an operating system (OS) such as Windows (registered trademark), a driver of a network adapter, and the like, as well as the above-described safety degree inspection program. The RAM (Random Access Memory) 33 appropriately stores programs executed by the CPU 31, data, and the like. The CPU 31, the ROM 32 and the RAM 33 are mutually connected by a bus 34.
 なお、サーバ11のCPU31(コンピュータ)が実行するプログラムは、本明細書で説明する順序に沿って時系列に処理が行われるプログラムであっても良いし、並列に、あるいは呼び出しが行われたとき等の必要なタイミングで個別に処理が行われるプログラムであっても良い。 Note that the program executed by the CPU 31 (computer) of the server 11 may be a program that performs processing in chronological order according to the order described in this specification, or when calls are performed in parallel or in parallel. It may be a program that is individually processed at necessary timing such as.
 CPU31にはまた、バス34を介して入出力インタフェース35が接続されている。入出力インタフェース35には、キーボード、マウス、マイクロホン等よりなる入力部36、ディスプレイ、スピーカ等よりなる出力部37が接続されている。CPU31は、入力部36から入力される指令に対応して各種の処理を実行する。そして、CPU31は、処理の結果を出力部37に出力する。 An input / output interface 35 is also connected to the CPU 31 via the bus 34. The input / output interface 35 is connected to an input unit 36 including a keyboard, a mouse, a microphone and the like, and an output unit 37 including a display, a speaker and the like. The CPU 31 executes various processes in response to the command input from the input unit 36. Then, the CPU 31 outputs the result of the process to the output unit 37.
 入出力インタフェース35にはまた、例えばハードディスクからなる記憶部38が接続されている。記憶部38は、CPU31が実行するプログラムや各種のデータを記憶する。なお、このプログラムは、通信部39により外部の装置から取得されるようにしてもよい。 The input / output interface 35 is also connected to a storage unit 38 formed of, for example, a hard disk. The storage unit 38 stores programs executed by the CPU 31 and various data. Note that this program may be acquired from an external device by the communication unit 39.
 また、入出力インタフェース35には、ネットワークを介して外部の装置と通信する通信部39とドライブ40が接続されている。ドライブ40は、磁気ディスク、光ディスク、光磁気ディスク、或いは半導体メモリなどのリムーバブルメディア41が装着されたとき、それらを駆動し、そこに記録されているプログラムやデータなどを取得する。取得されたプログラムやデータは、必要に応じて記憶部38に転送され、記憶される。 Further, to the input / output interface 35, a communication unit 39 for communicating with an external device through a network and a drive 40 are connected. When a removable medium 41 such as a magnetic disk, an optical disk, a magneto-optical disk, or a semiconductor memory is mounted, the drive 40 drives them and acquires programs and data recorded therein. The acquired program and data are transferred to and stored in the storage unit 38 as necessary.
 なお、図1の端末装置12のハードウェア構成も、サーバ11の構成と基本的に同様であるので、その説明については省略する。 The hardware configuration of the terminal device 12 of FIG. 1 is also basically the same as the configuration of the server 11, and thus the description thereof will be omitted.
<メイン画面の例>
 図3は、ユーザが端末装置12から、安全度検査プログラムが実行されたサーバ11にアクセスした際に、端末装置12のディスプレイ(ブラウザ)上に最初に表示されるメイン画面の例を示している。
<Example of main screen>
FIG. 3 shows an example of a main screen displayed first on a display (browser) of the terminal device 12 when the user accesses the server 11 on which the safety level inspection program is executed from the terminal device 12. .
 図3に示されるメイン画面は、基礎情報登録グループ、検査結果登録グループ、調査結果登録グループ、及び、結果閲覧グループの4つのグループに分類されている。 The main screen shown in FIG. 3 is classified into four groups of a basic information registration group, an examination result registration group, a survey result registration group, and a result browsing group.
 基礎情報登録グループは、安全検査を行う対象の会社名や商品名(検体名)などの基礎情報を登録するグループである。基礎情報登録グループには、サンプル情報登録ボタン61と、顧客マスターボタン62が含まれる。 The basic information registration group is a group for registering basic information such as a company name and a product name (specimen name) to be subjected to a safety inspection. The basic information registration group includes a sample information registration button 61 and a customer master button 62.
 サンプル情報登録ボタン61は、検査対象の商品(以下、検体ともいう。)を登録する際に、ユーザによって押下(操作)される。サンプル情報登録ボタン61が押下された場合、後述する図5のサンプル情報登録画面が表示される。 The sample information registration button 61 is pressed (operated) by the user when registering a product to be inspected (hereinafter, also referred to as a sample). When the sample information registration button 61 is pressed, a sample information registration screen of FIG. 5 described later is displayed.
 顧客マスターボタン62は、検査対象の会社、その会社の事業所や店舗などの施設など、顧客情報を登録する際に、ユーザによって押下される。顧客マスターボタン62が押下された場合、顧客名および施設名と、それらを一意に識別するコード番号などを入力する顧客登録画面が表示され、顧客登録画面で登録された内容が、顧客データベースとして記憶される。 The customer master button 62 is pressed by the user when registering customer information, such as a company to be inspected, facilities of the company or facilities of the company, and the like. When the customer master button 62 is pressed, a customer registration screen for inputting a customer name and a facility name, a code number uniquely identifying them, and the like is displayed, and the contents registered on the customer registration screen are stored as a customer database. Be done.
 検査結果登録グループは、検体の毒性や薬剤についての検査結果を登録(入力)するグループである。検査結果登録グループには、食中毒細菌結果登録ボタン71、農薬・抗生物質結果登録ボタン72、放射線測定結果登録ボタン73、異物混入検査結果登録ボタン74、アレルゲン混入検査結果登録ボタン75、および、ウイルス検査結果登録ボタン76が含まれる。 The test result registration group is a group that registers (inputs) test results on the toxicity and medicine of the sample. In the inspection result registration group, food poisoning bacteria result registration button 71, pesticide / antibiotic result registration button 72, radiation measurement result registration button 73, foreign substance contamination inspection result registration button 74, allergen contamination inspection result registration button 75, and virus inspection A result registration button 76 is included.
 食中毒細菌結果登録ボタン71は、検体の食中毒細菌検査の検査結果を登録する際に、ユーザによって押下される。食中毒細菌結果登録ボタン71が押下された場合、後述する図6の食中毒細菌検査結果登録画面が表示される。 The food poisoning bacteria result registration button 71 is pressed by the user when registering the test result of the food poisoning bacteria test of the sample. When the food poisoning bacteria result registration button 71 is pressed, a food poisoning bacteria test result registration screen of FIG. 6 described later is displayed.
 農薬・抗生物質結果登録ボタン72は、検体の農薬・抗生物質の含有量の検査結果を登録する際に、ユーザによって押下される。農薬・抗生物質結果登録ボタン72が押下された場合、後述する図7の農薬・抗生物質検査結果登録画面が表示される。 The pesticide / antibiotic result registration button 72 is pressed by the user when registering the test result of the content of the pesticide / antibiotic of the sample. When the pesticide / antibiotic result registration button 72 is pressed, the pesticide / antibiotic test result registration screen of FIG. 7 described later is displayed.
 放射線測定結果登録ボタン73は、検体の放射線量の検査結果を登録する際に、ユーザによって押下される。放射線測定結果登録ボタン73が押下された場合、後述する図11の放射線測定結果登録画面が表示される。 The radiation measurement result registration button 73 is pressed by the user when registering the inspection result of the radiation dose of the sample. When the radiation measurement result registration button 73 is pressed, a radiation measurement result registration screen of FIG. 11 described later is displayed.
 異物混入検査結果登録ボタン74は、検体の異物混入検査の検査結果を登録する際に、ユーザによって押下される。異物混入検査結果登録ボタン74が押下された場合、後述する図12の異物混入検査結果登録画面が表示される。 The foreign substance contamination inspection result registration button 74 is pressed by the user when registering the inspection result of the foreign substance contamination inspection of the sample. When the foreign substance contamination inspection result registration button 74 is pressed, a foreign substance contamination inspection result registration screen of FIG. 12 described later is displayed.
 アレルゲン混入検査結果登録ボタン75は、検体のアレルゲン混入検査の検査結果を登録する際に、ユーザによって押下される。アレルゲン混入検査結果登録ボタン75が押下された場合、後述する図13のアレルゲン混入検査結果登録画面が表示される。 The allergen contamination test result registration button 75 is pressed by the user when registering the test result of the allergen contamination test of the sample. When the allergen contamination test result registration button 75 is pressed, the allergen contamination test result registration screen of FIG. 13 described later is displayed.
 ウイルス検査結果登録ボタン76は、検体および従事者に対するノロウイルス検査の検査結果を登録する際に、ユーザによって押下される。ウイルス検査結果登録ボタン76が押下された場合、後述する図14のウイルス検査結果登録画面が表示される。 The virus test result registration button 76 is pressed by the user when registering the test result of the norovirus test on the sample and the worker. When the virus test result registration button 76 is pressed, a virus test result registration screen of FIG. 14 described later is displayed.
 調査結果登録グループは、検体を扱う従事者や施設の衛生についての調査結果を登録するグループである。調査結果登録グループには、健康管理調査結果登録ボタン81、感染予防対策調査結果登録ボタン82、身なり・服装・髪型・装飾調査結果登録ボタン83、および衛生教育調査結果登録ボタン84が含まれる。 The survey result registration group is a group that registers survey results on the hygiene of workers and facilities that handle specimens. The survey result registration group includes a health management survey result registration button 81, an infection prevention countermeasure survey result registration button 82, a personal appearance / dress / hair style / decoration survey result registration button 83, and a hygiene education survey result registration button 84.
 健康管理調査結果登録ボタン81は、個人で管理するレベルの健康管理について、従事者に調査した結果を登録する際に、ユーザによって押下される。健康管理調査結果登録ボタン81が押下された場合、後述する図15の健康管理調査結果登録画面が表示される。 The health management survey result registration button 81 is pressed by the user when registering the result of survey on the worker regarding the level of health management managed by the individual. When the health management research result registration button 81 is pressed, a health management research result registration screen of FIG. 15 described later is displayed.
 感染予防対策調査結果登録ボタン82は、施設の感染予防対策を調査した結果を登録する際に、ユーザによって押下される。感染予防対策調査結果登録ボタン82が押下された場合、後述する図16の感染予防対策調査結果登録画面が表示される。 The infection prevention countermeasure research result registration button 82 is pressed by the user when registering the result of investigating the infection prevention countermeasure of the facility. When the infection prevention countermeasure research result registration button 82 is pressed, an infection prevention countermeasure research result registration screen of FIG. 16 described later is displayed.
 身なり・服装・髪型・装飾調査結果登録ボタン83は、従事者の身なり・服装・髪型・装飾について調査した結果を登録する際に、ユーザによって押下される。身なり・服装・髪型・装飾調査結果登録ボタン83が押下された場合、後述する図17の身なり・服装・髪型・装飾調査結果登録画面が表示される。 The appearance / dress / haircut / decoration research result registration button 83 is pressed by the user when registering the result of investigation on the appearance / dress / haircut / decoration of the worker. When the appearance / dress / haircut / decoration research result registration button 83 is pressed, the appearance / dress / hairstyle / modification research result registration screen of FIG. 17 described later is displayed.
 衛生教育調査結果登録ボタン84は、衛生教育の体制や従事者の理解度についての調査結果を登録する際に、ユーザによって押下される。衛生教育調査結果登録ボタン84が押下された場合、後述する図18の衛生教育調査結果登録画面が表示される。 The hygiene education research result registration button 84 is pressed by the user when registering the research result on the health education system and the degree of understanding of the worker. When the hygiene education research result registration button 84 is pressed, a hygiene education research result registration screen of FIG. 18 described later is displayed.
 結果閲覧グループは、検体の検査結果を出力するグループである。結果閲覧グループには、結果一覧ボタン91と、結果出力ボタン92が含まれる。 The result browsing group is a group that outputs the test results of the sample. The result browsing group includes a result list button 91 and a result output button 92.
 結果一覧ボタン91は、検体の各検査項目の検査・調査結果の一覧を表示する際に、ユーザによって押下される。結果一覧ボタン91が押下された場合、後述する図19の結果一覧画面が表示される。 The result list button 91 is pressed by the user when displaying a list of examination / survey results of each examination item of the sample. When the result list button 91 is pressed, a result list screen of FIG. 19 described later is displayed.
 結果出力ボタン92は、検体についての検査結果および調査結果に基づく最終的な安全度の判定結果を表示する際に、ユーザによって押下される。結果出力ボタン92が押下された場合、後述する図20の結果出力画面が表示される。 The result output button 92 is pressed by the user when displaying the final safety determination result based on the examination result and the examination result of the sample. When the result output button 92 is pressed, the result output screen of FIG. 20 described later is displayed.
<安全度スケールシステムの機能構成ブロック図>
 図4は、安全度検査プログラムがサーバ11で実行されることにより実現される、安全度スケールシステム1の機能的構成例を示すブロック図である。
<Functional block diagram of safety scale system>
FIG. 4 is a block diagram showing an example of a functional configuration of the safety degree scale system 1 realized by the safety degree inspection program being executed by the server 11.
 安全度スケールシステム1は、基礎情報登録部101、検査結果登録部102、調査結果登録部103、リスク影響度判定部104、リスク発生頻度判定部105、安全度算出部106、結果出力部107、および登録DB108により構成される。 The safety degree scale system 1 includes a basic information registration unit 101, an examination result registration unit 102, a survey result registration unit 103, a risk influence degree judgment unit 104, a risk occurrence frequency judgment unit 105, a safety degree calculation unit 106, a result output unit 107. And a registration DB 108.
 基礎情報登録部101は、図3のメイン画面において、基礎情報登録グループに属するサンプル情報登録ボタン61と顧客マスターボタン62が押下された場合の処理を実行する。 The basic information registration unit 101 executes processing when the sample information registration button 61 and the customer master button 62 belonging to the basic information registration group are pressed on the main screen of FIG. 3.
 検査結果登録部102は、図3のメイン画面において、検査結果登録グループに属する、食中毒細菌結果登録ボタン71、農薬・抗生物質結果登録ボタン72、放射線測定結果登録ボタン73、異物混入検査結果登録ボタン74、アレルゲン混入検査結果登録ボタン75、および、ウイルス検査結果登録ボタン76が押下された場合の処理を実行する。 The examination result registration unit 102 belongs to the examination result registration group on the main screen of FIG. 3 and includes the food poisoning bacteria result registration button 71, the agrochemical / antibiotic result registration button 72, the radiation measurement result registration button 73, and the foreign matter contamination inspection result registration button 74, the processing when the allergen contamination test result registration button 75 and the virus test result registration button 76 are pressed is executed.
 調査結果登録部103は、調査結果登録グループに属する、健康管理調査結果登録ボタン81、感染予防対策調査結果登録ボタン82、身なり・服装・髪型・装飾調査結果登録ボタン83、および衛生教育調査結果登録ボタン84が押下された場合の処理を実行する。 The survey result registration unit 103 belongs to a survey result registration group, and includes a health management survey result registration button 81, an infection prevention countermeasure survey result registration button 82, a personal appearance / dress / hair style / decorative survey result registration button 83, and a hygiene education survey result registration. A process when the button 84 is pressed is executed.
 リスク影響度判定部104は、検査結果登録グループおよび調査結果登録グループで登録された検査結果および調査結果に基づいて、健康被害に対する検体のリスクの影響度を判定する。リスクの影響度の判定方法の詳細は後述する。 The risk influence degree determination unit 104 determines the degree of influence of the risk of the sample on the health damage based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Details of the method of determining the degree of risk influence will be described later.
 リスク発生頻度判定部105は、検査結果登録グループおよび調査結果登録グループで登録された検査結果および調査結果に基づいて、健康被害に対する検体のリスクの発生頻度を判定する。リスクの発生頻度の判定方法の詳細は後述する。 The risk occurrence frequency determination unit 105 determines the occurrence frequency of the risk of the sample to the health damage based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Details of the method of determining the risk occurrence frequency will be described later.
 安全度算出部106は、リスク影響度判定部104で判定されたリスクの影響度と、リスク発生頻度判定部105で判定されたリスクの発生頻度とを用いて、リスクの大きさを算出し、算出されたリスクの大きさから、健康被害に対する安全度を算出する。詳細は後述するが、健康被害に対する安全度は、算出されたリスクの大きさの逆数で算出される。 The safety degree calculation unit 106 calculates the magnitude of the risk using the degree of impact of the risk determined by the risk degree of impact determination unit 104 and the occurrence frequency of the risk determined by the risk occurrence frequency determination unit 105, From the calculated magnitude of risk, calculate the degree of safety against health damage. Although the details will be described later, the degree of safety against health damage is calculated by the reciprocal of the calculated magnitude of risk.
 結果出力部107は、図3のメイン画面において、結果閲覧グループに属する結果一覧ボタン91と結果出力ボタン92が押下された場合の処理を実行する。 The result output unit 107 executes processing when the result list button 91 and the result output button 92 belonging to the result browsing group are pressed on the main screen of FIG. 3.
 登録DB108は、基礎情報登録部101、検査結果登録部102、調査結果登録部103等で登録された情報、および、安全度算出部106等で算出された結果等を記憶する。顧客データベースは、登録DB108に記憶されているデータベースの一つである。 The registration DB 108 stores information registered by the basic information registration unit 101, the inspection result registration unit 102, the survey result registration unit 103 and the like, and the result calculated by the safety degree calculation unit 106 and the like. The customer database is one of the databases stored in the registration DB 108.
 基礎情報登録部101、検査結果登録部102、調査結果登録部103、および結果出力部107は、サーバ11および端末装置12のディスプレイに所定の画面を表示させる表示制御部や、サーバ11および端末装置12のキーボードやマウス等から入力された入力情報を取得する情報取得部、サーバ11および端末装置12間の通信を制御する通信制御部を、個別または共通に有している。 The basic information registration unit 101, the examination result registration unit 102, the investigation result registration unit 103, and the result output unit 107 are a display control unit for displaying a predetermined screen on the display of the server 11 and the terminal device 12, the server 11 and the terminal device An information acquisition unit that acquires input information input from a keyboard, a mouse or the like 12 and a communication control unit that controls communication between the server 11 and the terminal device 12 are individually or commonly provided.
 以下、メイン画面の各ボタンが押下されたときの処理(動作)と、入力された検査結果および調査結果に基づく安全度の算出について詳しく説明する。 Hereinafter, the process (operation) when each button on the main screen is pressed, and the calculation of the degree of safety based on the input inspection result and investigation result will be described in detail.
<サンプル情報登録画面>
 図5は、サンプル情報登録画面の例を示している。
<Sample information registration screen>
FIG. 5 shows an example of the sample information registration screen.
 ユーザは、検査対象の商品(検体)を新たに登録する場合、図3のメイン画面において、サンプル情報登録ボタン61を押下する。これにより、図5のサンプル情報登録画面が表示される。 When newly registering a product (sample) to be examined, the user presses the sample information registration button 61 on the main screen of FIG. 3. Thereby, the sample information registration screen of FIG. 5 is displayed.
 サンプル情報登録画面では、顧客名121、施設名122、施設CD123、サブCD124、検体名125、検体ID126、検査127、および調査128の各項目と、登録ボタン129、修正ボタン130、およびキャンセルボタン131が表示される。 In the sample information registration screen, each item of customer name 121, facility name 122, facility CD 123, sub CD 124, sample name 125, sample ID 126, test 127, and survey 128, registration button 129, correction button 130, and cancel button 131 Is displayed.
 サンプル情報登録画面の顧客名121、施設名122、検体名125の項目には、それぞれ、顧客の会社名、店舗や事業所の施設名、検査対象の商品名が、ユーザによって入力される。検体名125の項目には、例えば、図5に示されるように「ケーキ」などの検査対象の食品の名前が入力される。 In the fields of customer name 121, facility name 122, and sample name 125 on the sample information registration screen, the company name of the customer, the facility name of the store or business place, and the product name to be inspected are input by the user. In the item of the sample name 125, for example, as shown in FIG. 5, the name of the food to be tested such as "cake" is input.
 顧客の会社名および施設名は、直接入力してもよいし、顧客マスターボタン62の押下で表示される顧客登録画面で入力された顧客データベースに基づいて、会社名や施設名がプルダウンで選択入力できるようになっていてもよい。 The company name and facility name of the customer may be directly input, or based on the customer database input on the customer registration screen displayed when the customer master button 62 is pressed, the company name and facility name are selected and input by pull-down. It may be possible.
 顧客名121および施設名122の項目に顧客の会社名および施設名が入力されると、それに対応して、施設CD123およびサブCD124の項目には、顧客データベースから、入力された会社名および施設名を一意に識別するコード番号(CD)が表示される。 When the customer's company name and facility name are entered in the items of customer name 121 and facility name 122, the company name and facility name entered from the customer database are entered in the items of facility CD 123 and sub CD 124 correspondingly. The code number (CD) that uniquely identifies is displayed.
 また、検体ID126の項目は、サンプル情報登録画面の初期状態では、空欄になっている。顧客名121、施設名122、検体名125の各項目が入力され、登録ボタン129が押下されたときに、基礎情報登録部101によって検体IDが付与され、登録DB108に記憶される。 The item of the sample ID 126 is blank in the initial state of the sample information registration screen. When each item of the customer name 121, the facility name 122, and the sample name 125 is input and the registration button 129 is pressed, a sample ID is assigned by the basic information registration unit 101 and stored in the registration DB.
 既に登録DB108に登録されている検体の登録情報を修正したい場合には、修正ボタン130が押下される。修正ボタン130が押下されると、登録DB108に登録されている検体を選択する画面(不図示)が表示され、所定の検体が選択されると、選択された検体についての登録情報が読み出され、サンプル情報登録画面に表示される。この場合、検体ID126の項目には、既に割り当てられている検体IDが表示される。 When it is desired to correct the registration information of the sample already registered in the registration DB 108, the correction button 130 is pressed. When the correction button 130 is pressed, a screen (not shown) for selecting a sample registered in the registration DB 108 is displayed, and when a predetermined sample is selected, registration information on the selected sample is read out. , Is displayed on the sample information registration screen. In this case, the sample ID already assigned is displayed in the item of the sample ID 126.
 検査127の項目には、検査結果登録グループに属する各検査に対応するボタン、すなわち、食中毒細菌(毒素)ボタン132、放射線測定ボタン133、ウイルス検査ボタン134、異物混入ボタン135、農薬・抗生物質ボタン136、及び、アレルゲン混入ボタン137が表示されている。 The items of inspection 127 are buttons corresponding to each inspection belonging to the inspection result registration group, that is, food poisoning bacteria (toxin) button 132, radiation measurement button 133, virus inspection button 134, foreign matter contamination button 135, pesticide / antibiotics button 136 and an allergen mixing button 137 are displayed.
 検査結果登録グループに属する各検査に対応するボタン132乃至137を押下すると、各検査の検査内容の詳細を設定する設定画面が表示される。また、検査127の項目のボタン132乃至137は、検査が既に終了し、検査結果が登録されている場合と、検査が未実施である場合とで、異なる色などにより区別されて表示される。これにより、検体ID126で識別される検体について、検査127の項目のなかのどの検査が終了済みであるかが一目で分かるようになっている。 When the buttons 132 to 137 corresponding to the respective examinations belonging to the examination result registration group are pressed, a setting screen for setting details of examination contents of the respective examinations is displayed. Further, the buttons 132 to 137 of the item of the examination 127 are distinguished and displayed in different colors or the like in the case where the examination is already finished and the examination result is registered and the case where the examination is not performed. As a result, for the sample identified by the sample ID 126, it is possible to see at a glance which test of the items of the test 127 has been completed.
 調査128の項目には、調査結果登録グループに属する各調査に対応するボタン、すなわち、健康管理(個人管理)ボタン141、感染予防対策(施設内)ボタン142、身なり・服装・髪型・装飾ボタン143、及び、衛生教育(知識)ボタン144が表示されている。 The items of survey 128 are buttons corresponding to each survey belonging to the survey result registration group, that is, health management (personal management) button 141, infection prevention measures (within facility) button 142, appearance, clothes, hairstyle, decoration button 143 And a hygiene education (knowledge) button 144 is displayed.
 調査結果登録グループに属する各調査に対応するボタン141乃至144を押下すると、各調査の調査内容の詳細を設定する設定画面が表示される。また、調査128の項目のボタン141乃至144は、調査が既に終了し、調査結果が登録されている場合と、調査が未実施である場合とで、異なる色などにより区別されて表示される。これにより、検体ID126で識別される検体について、調査128の項目のなかのどの調査が終了しているかが一目で分かるようになっている。 When the buttons 141 to 144 corresponding to each survey belonging to the survey result registration group are pressed, a setting screen for setting details of survey contents of each survey is displayed. In addition, the buttons 141 to 144 of the items of the survey 128 are distinguished and displayed in different colors or the like depending on whether the survey has already been completed and the survey results have been registered and the survey has not been performed. As a result, for the sample identified by the sample ID 126, it is possible to know at a glance which of the items of the survey 128 has been completed.
 登録ボタン129は、入力した情報を登録DB108に登録(修正)し、図3のメイン画面に戻る場合に押下される。キャンセルボタン131は、サンプル情報登録画面における情報の登録をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 129 is pressed when registering (correcting) the input information in the registration DB 108 and returning to the main screen of FIG. 3. The cancel button 131 is pressed to cancel the registration of information on the sample information registration screen and to return to the main screen of FIG.
<食中毒細菌検査結果登録画面>
 図6は、食中毒細菌検査結果登録画面の例を示している。
<Food poisoning bacteria test result registration screen>
FIG. 6 shows an example of the food poisoning bacteria test result registration screen.
 ユーザは、検体の食中毒細菌検査の検査結果を登録する場合、図3のメイン画面の食中毒細菌結果登録ボタン71を押下する。これにより、図6の食中毒細菌検査結果登録画面が表示される。 The user presses the food poisoning bacteria result registration button 71 on the main screen of FIG. 3 when registering the test result of the food poisoning bacteria test of the sample. Thereby, the food poisoning bacteria test result registration screen of FIG. 6 is displayed.
 食中毒細菌検査結果登録画面では、検体ID151および検査回数152の各項目と、検査結果入力欄153、並びに、登録ボタン154およびキャンセルボタン155が表示される。 On the food poisoning bacteria test result registration screen, each item of the sample ID 151 and the test count 152, a test result input field 153, and a registration button 154 and a cancel button 155 are displayed.
 検体ID151の項目には、食中毒細菌検査の検査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 151, the sample ID of the sample for which the test result of the food poisoning bacteria test is registered is displayed. The sample ID is specified by the user.
 検査回数152の項目には、検査対象期間のなかでの検査回数が表示される。本実施の形態では、検査対象期間は1週間であるとして説明する。図6の例では、検査回数として「4回」が表示されており、この場合、検査対象期間に指定された1週間のなかで、製造日(ロット)を変えて、4回の食中毒細菌検査が実施される。なお、検査回数は、図5のサンプル情報登録画面の食中毒細菌(毒素)ボタン132を押下して表示される設定画面で設定することができる。 In the item of the number of examinations 152, the number of examinations in the examination target period is displayed. In the present embodiment, the inspection target period is described as one week. In the example of FIG. 6, "4 times" is displayed as the number of tests, and in this case, food poisoning bacteria tests are performed 4 times by changing the production date (lot) within one week specified in the test period. Will be implemented. The number of examinations can be set on the setting screen displayed by pressing the food poisoning bacteria (toxin) button 132 on the sample information registration screen of FIG.
 検査結果入力欄153には、検査回数152の項目に表示されている検査回数分の結果入力欄が表示される。検査項目は、一般生菌、大腸菌群、カビ、酵母、黄色ブドウ球菌、セレウス、大腸菌、サルモネラ、腸炎ビブリオ、及び、耐熱性菌の10種類となっている。食中毒細菌検査の検査項目は、図5のサンプル情報登録画面の食中毒細菌(毒素)ボタン132を押下して表示される設定画面で設定することができる。一般生菌と大腸菌群は、菌検出数が1×10以下であれば問題なく、その他の菌類は、検出結果が陰性(-)または陽性(+)で表され、陰性(-)であれば問題がないと判定される。 In the inspection result input column 153, result input columns for the number of inspections displayed in the item of the number of inspections 152 are displayed. Test items are 10 types of general living bacteria, coliform bacteria, mold, yeast, Staphylococcus aureus, cereus, Escherichia coli, salmonella, Vibrio parahaemolyticus, and thermostable bacteria. The test items of the food poisoning bacteria test can be set on the setting screen displayed by pressing the food poisoning bacteria (toxin) button 132 of the sample information registration screen of FIG. There is no problem if the number of bacteria detected is 1 × 10 7 or less, and the other fungi are indicated as negative (-) or positive (+) if the number of bacteria detected is 1 × 10 7 or less. It is determined that there is no problem.
 登録ボタン154は、食中毒細菌検査の検査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン155は、食中毒細菌検査の検査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 154 is pressed to register (save) after inputting the test result of the food poisoning bacteria test. The cancel button 155 is pressed to cancel the input of the test result of the food poisoning bacteria test and return to the main screen of FIG.
<農薬・抗生物質検査結果登録画面>
 図7は、農薬・抗生物質検査結果登録画面の例を示している。
<Pesticide / antibiotic inspection result registration screen>
FIG. 7 shows an example of the pesticide / antibiotic test result registration screen.
 ユーザは、検体の農薬・抗生物質の含有量の検査結果を登録する場合、図3のメイン画面の農薬・抗生物質結果登録ボタン72を押下する。これにより、図7の農薬・抗生物質検査結果登録画面が表示される。 The user presses the pesticide / antibiotic result registration button 72 on the main screen of FIG. 3 when registering the inspection result of the content of the pesticide / antibiotic of the sample. As a result, the pesticide / antibiotic test result registration screen of FIG. 7 is displayed.
 農薬・抗生物質検査結果登録画面では、検体ID161、検査結果入力欄162、登録ボタン163、およびキャンセルボタン164が表示される。 In the agrochemical / antibiotic test result registration screen, a sample ID 161, a test result input field 162, a registration button 163, and a cancel button 164 are displayed.
 検体ID161の項目には、農薬・抗生物質検査の検査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 161, the sample ID of the sample for registering the test result of the agrochemical / antibiotic test is displayed. The sample ID is specified by the user.
 検査結果入力欄162には、検査対象に設定されている農薬・抗生物質の項目の結果入力欄が表示される。図7の例では、「1,1-ジクロロ-2,2-ビス(4-エチルフェニル)エタン」、「1,2-ジブロモエタン」、「1-ナフタレン酢酸」、「2-(10.01ナフチル)アセタミド」、「2,2-DPA(ダラポン)」、・・・など22項目の農薬・抗生物質が検査対象に設定され、検査結果が入力可能になっている。基準値以上の値が検出された場合には、その検出結果の値が入力され、検出結果が未検出(検出不可のレベル)である場合には「ND(NO DETECT)」が入力される。 In the test result input column 162, a result input column of the items of the agrochemical and the antibiotic which are set as the test target is displayed. In the example of FIG. 7, “1,1-dichloro-2,2-bis (4-ethylphenyl) ethane”, “1,2-dibromoethane”, “1-naphthaleneacetic acid”, “2- (10.01) 22 items of pesticides / antibiotics such as Naphthyl) Acetamide, "2, 2-DPA (Darapon)", ... are set as test targets, and test results can be input. If a value equal to or greater than the reference value is detected, the value of the detection result is input, and if the detection result is undetected (undetectable level), “ND (NO DETECT)” is input.
 検査対象とする農薬・抗生物質は、図5のサンプル情報登録画面の農薬・抗生物質ボタン136を押下して表示される設定画面で設定することができる。検査対象として設定可能な農薬・抗生物質は、図8乃至図10に示される約460項目である。 The pesticide / antibiotic to be tested can be set on the setting screen displayed by pressing the pesticide / antibiotic button 136 on the sample information registration screen of FIG. The pesticides / antibiotics that can be set as the test target are about 460 items shown in FIG. 8 to FIG.
<放射線測定結果登録画面>
 図11は、放射線測定結果登録画面の例を示している。
<Radiation measurement result registration screen>
FIG. 11 shows an example of a radiation measurement result registration screen.
 ユーザは、検体の放射線量の検査結果を登録する場合、図3のメイン画面の放射線測定結果登録ボタン73を押下する。これにより、図11の放射線測定結果登録画面が表示される。 When registering the examination result of the radiation dose of the sample, the user presses the radiation measurement result registration button 73 on the main screen of FIG. 3. Thereby, the radiation measurement result registration screen of FIG. 11 is displayed.
 放射線測定結果登録画面では、検体ID171および検査回数172の各項目と、測定結果入力欄173、並びに、登録ボタン174およびキャンセルボタン175が表示される。 On the radiation measurement result registration screen, each item of the sample ID 171 and the number of times of examination 172, a measurement result input field 173, a registration button 174 and a cancel button 175 are displayed.
 検体ID171の項目には、放射線測定の測定結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 171, the sample ID of the sample for which the measurement result of the radiation measurement is registered is displayed. The sample ID is specified by the user.
 検査回数172の項目には、検査対象期間に指定された1週間のなかでの測定回数が表示される。この例では、検査回数として「3回」が表示されており、この場合、検査対象期間に指定された1週間のなかで、日にちを変えて、3回の放射線測定が実施される。検査回数は、図5のサンプル情報登録画面の放射線測定ボタン133を押下して表示される設定画面で設定することができる。 In the item of the number of examinations 172, the number of measurements in one week designated in the examination target period is displayed. In this example, “three times” is displayed as the number of examinations, and in this case, radiation measurement is performed three times while changing the date within one week designated as the examination target period. The number of examinations can be set on the setting screen displayed by pressing the radiation measurement button 133 on the sample information registration screen of FIG.
 測定結果入力欄173には、検査回数172の項目に表示されている検査回数分の結果入力欄が表示される。測定項目は、セシウム137およびセシウム134である。測定値が10ベクレル/kg未満である場合は正常(問題なし)、測定値が10ベクレル/kg以上である場合は異常(NG)と判定され、入力される。なお、セシウム137とセシウム134の測定値の合算値で正常か否かの判定を行ってもよい。 In the measurement result input column 173, result input columns corresponding to the number of inspections displayed in the item of the number of inspections 172 are displayed. The measurement items are cesium 137 and cesium 134. If the measured value is less than 10 BEC / kg, it is judged as normal (no problem), and if the measured value is 10 BEC / kg or more, it is judged as abnormal (NG) and input. In addition, you may determine whether it is normal by the sum total of the measured value of cesium 137 and cesium 134. As shown in FIG.
 登録ボタン174は、放射線測定の測定結果を入力後、登録(保存)する場合に押下される。キャンセルボタン175は、放射線測定の測定結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 174 is pressed to register (save) after the measurement result of the radiation measurement is input. The cancel button 175 is pressed when canceling the input of the measurement result of the radiation measurement and returning to the main screen of FIG.
<異物混入検査結果登録画面>
 図12は、異物混入検査結果登録画面の例を示している。
<Foreign matter contamination inspection result registration screen>
FIG. 12 shows an example of the foreign substance contamination inspection result registration screen.
 ユーザは、検体の異物混入検査の検査結果を登録する場合、図3のメイン画面の異物混入検査結果登録ボタン74を押下する。これにより、図12の異物混入検査結果登録画面が表示される。 When registering the inspection result of the foreign substance contamination inspection of the sample, the user presses the foreign substance contamination inspection result registration button 74 on the main screen of FIG. 3. Thereby, the foreign substance contamination inspection result registration screen of FIG. 12 is displayed.
 異物混入検査結果登録画面では、検体ID181および検査回数182の各項目と、検査結果入力欄183、発生頻度入力欄184、コメント入力欄185、総合結果表示欄186、並びに、登録ボタン187およびキャンセルボタン188が表示される。 In the foreign substance contamination test result registration screen, each item of the sample ID 181 and the test frequency 182, the test result input column 183, the occurrence frequency input column 184, the comment input column 185, the comprehensive result display column 186, the registration button 187 and the cancel button 188 is displayed.
 検体ID181の項目には、異物混入検査の検査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 Under the item of the sample ID 181, the sample ID of the sample for which the test result of the foreign substance contamination test is registered is displayed. The sample ID is specified by the user.
 検査回数182の項目には、検査対象期間に指定された1週間のなかでの検査回数が表示される。この例では、検査回数として「1回」が表示されており、この場合、検査対象期間に指定された1週間のなかで1回の異物混入検査が実施される。検査回数は、図5のサンプル情報登録画面の異物混入ボタン135を押下して表示される設定画面で設定することができる。 In the item of the number of examinations 182, the number of examinations in one week designated in the examination target period is displayed. In this example, "one" is displayed as the number of inspections, and in this case, one foreign substance contamination inspection is performed within one week designated in the inspection target period. The number of inspections can be set on the setting screen displayed by pressing the foreign substance mixing button 135 on the sample information registration screen of FIG.
 検査結果入力欄183には、異物混入検査の各検査項目、具体的には、「X線検出器」、「個人装備」、「外気汚染」、「昆虫飛来」、「防鼠対策」、「設備老朽具合」、「清掃頻度」、「改善チームの有無」、及び「製品保存状態」が表示されている。この検査項目も、図5のサンプル情報登録画面の異物混入ボタン135を押下して表示される設定画面で設定することができる。 In the inspection result input column 183, each inspection item of the foreign substance contamination inspection, specifically, "X-ray detector", "personal equipment", "open air pollution", "insect flying", "anti-corrosion measures", " The status of equipment deterioration, "cleaning frequency", "presence of improvement team", and "product storage state" are displayed. This inspection item can also be set on the setting screen displayed by pressing the alien substance mixing button 135 on the sample information registration screen of FIG.
 検査結果入力欄183の各検査項目は、例えば、トグルボタンとなっており、押下するごとに、[OK]と[NG]の表示が切り替わる。検査結果入力欄183の各検査項目に対して、[OK]または[NG]のいずれかが入力される。 Each inspection item in the inspection result input column 183 is, for example, a toggle button, and the display of [OK] and [NG] is switched each time the inspection button is pressed. For each inspection item in the inspection result input field 183, either [OK] or [NG] is input.
 「X線検出器」の項目は、施設に異物を検出するための金属探知機が備えてあり、正常に使用可能であるかを検査する検査項目である。「個人装備」の項目は、個人装備についての規定があるかを検査する検査項目である。「外気汚染」の項目は、外気汚染があるかを検査する検査項目である。「昆虫飛来」の項目は、昆虫飛来対策(昆虫対策)があるかを検査する検査項目である。「防鼠対策」は、鼠対策があるかを検査する検査項目である。「設備老朽具合」の項目は、設備のメンテナンスが行き届いているかを検査する検査項目である。「清掃頻度」の項目は、清掃記録があるかを検査する検査項目である。「改善チームの有無」の項目は、改善チームなど、改善事項チームを社内(施設、事業所)で規定しており、その実行記録があるかを検査する検査項目である。「製品保存状態」の項目は、製品若しくは原料の保管状態が適切かを検査する検査項目である。 The item "X-ray detector" is an inspection item for checking whether the facility is equipped with a metal detector for detecting foreign matter and can be used normally. The item of "personal equipment" is an inspection item to check whether there is a provision for personal equipment. The item "outside air pollution" is an inspection item for inspecting whether there is outside air pollution. The item "Insect flying" is an inspection item for testing whether there is an insect flying countermeasure (insect countermeasure). "Anti-corrosion measures" is an inspection item to check if there is a plagiarism measure. The item of “Aging condition of equipment” is an inspection item for inspecting whether the maintenance of the equipment is in good condition. The item "cleaning frequency" is an inspection item for inspecting whether there is a cleaning record. The item of "presence of improvement team" is an inspection item which defines improvement team, such as improvement team, in-house (facility, business establishment) and checks whether or not the execution record is present. The item of "product storage state" is an inspection item for checking whether the storage state of the product or the raw material is appropriate.
 発生頻度入力欄184には、異物混入の発生頻度を、ユーザが従事者にヒアリングを行った結果が入力される。発生頻度入力欄184は、例えば、毎日起こる、毎週起こる、毎月起こる、数か月に1回起こる、または、半年以上発生していない、のなかから、いずれかを選択して入力するようになっている。 In the occurrence frequency input field 184, the result of the user interviewing the worker with the occurrence frequency of the foreign matter contamination is input. For example, the occurrence frequency input field 184 is to select and enter any of daily occurrence, weekly occurrence, monthly occurrence, monthly occurrence, or no occurrence for more than half a year. ing.
 検査結果入力欄183の各検査項目で、[NG]とした項目については、コメント入力欄185に、[NG]とした理由、改善事項などがコメントとして入力される。総合結果表示欄186には、検査結果入力欄183の各検査項目に基づく総合判定結果(OK、NG)が表示される。例えば、検査結果入力欄183の各検査項目のなかで一つでも[NG]の項目がある場合には、総合判定結果はNGと判定される。 For each inspection item in the inspection result input column 183, for the item “NG”, the reason for setting “NG” in the comment input column 185, an improvement item, etc. are input as a comment. In the integrated result display column 186, integrated judgment results (OK, NG) based on each inspection item of the inspection result input column 183 are displayed. For example, when there is an item of [NG] even in one or more inspection items of the inspection result input column 183, the comprehensive determination result is determined as NG.
 登録ボタン187は、異物混入検査の検査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン188は、異物混入検査の検査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 187 is pressed when registering (saving) after the inspection result of the foreign substance contamination inspection is input. The cancel button 188 is pressed to cancel the input of the inspection result of the foreign substance contamination inspection and to return to the main screen of FIG. 3.
<アレルゲン混入検査結果登録画面>
 図13は、アレルゲン混入検査結果登録画面の例を示している。
<Allergen contamination test result registration screen>
FIG. 13 shows an example of the allergen contamination test result registration screen.
 ユーザは、検体のアレルゲン混入検査の検査結果を登録する場合、図3のメイン画面のアレルゲン混入検査結果登録ボタン75を押下する。これにより、図13のアレルゲン混入検査結果登録画面が表示される。 When registering the test result of the allergen contamination test of the sample, the user presses the allergen contamination test result registration button 75 on the main screen of FIG. 3. Thereby, the allergen contamination test result registration screen of FIG. 13 is displayed.
 アレルゲン混入検査結果登録画面では、検体ID191および検査回数192の各項目と、検査結果入力欄193、並びに、登録ボタン194およびキャンセルボタン195が表示される。 On the allergen contamination test result registration screen, each item of the sample ID 191 and the test count 192, a test result input column 193, a registration button 194 and a cancel button 195 are displayed.
 検体ID191の項目には、アレルゲン混入検査の検査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 191, the sample ID of the sample for which the test result of the allergen contamination test is registered is displayed. The sample ID is specified by the user.
 検査回数192の項目には、検査対象期間に指定された1週間のなかでの検査回数が表示される。この例では、検査回数として「3回」が表示されており、この場合、検査対象期間に指定された1週間のなかで、日にちを変えて、3回のアレルゲン混入検査が実施される。検査回数は、図5のサンプル情報登録画面のアレルゲン混入ボタン137を押下して表示される設定画面で設定することができる。 In the item of the number of examinations 192, the number of examinations in one week designated in the examination target period is displayed. In this example, “three times” is displayed as the number of examinations, and in this case, three days of the allergen contamination examination are performed by changing the date within one week designated in the examination target period. The number of examinations can be set on the setting screen displayed by pressing the allergen mixing button 137 on the sample information registration screen of FIG.
 検査結果入力欄193には、検査回数192の項目に表示されている検査回数分の結果入力欄が表示される。アレルゲン混入検査の検査項目は、そば、小麦、落花生、牛乳、卵、および甲殻類(えび、かに)の表示義務のある6項目である。なお、検査項目は、図5のサンプル情報登録画面のアレルゲン混入ボタン137を押下して表示される設定画面で設定可能である。アレルゲン混入物質が0.1ppm以上検出された場合、検出結果として陽性(+)が入力され、0.1ppm未満である場合、陰性(-)が入力される。検出結果の全てが陰性(-)であれば問題がないと判定される。 In the inspection result input column 193, result input columns corresponding to the number of inspections displayed in the item of the number of inspections 192 are displayed. The test items of the allergen contamination test are six items that are required to display buckwheat, wheat, peanuts, milk, eggs, and crustacea (shrimp, crab). The inspection item can be set on the setting screen displayed by pressing the allergen mixing button 137 on the sample information registration screen of FIG. If an allergen contaminant is detected at 0.1 ppm or more, a positive (+) is input as a detection result, and if it is less than 0.1 ppm, a negative (-) is input. If all the detection results are negative (-), it is determined that there is no problem.
 登録ボタン194は、アレルゲン混入検査の検査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン195は、アレルゲン混入検査の検査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 194 is pressed to register (save) after inputting the test result of the allergen contamination test. The cancel button 195 is pressed to cancel the input of the test result of the allergen contamination test and to return to the main screen of FIG. 3.
<ウイルス検査結果登録画面>
 図14は、ウイルス検査結果登録画面の例を示している。
<Virus test result registration screen>
FIG. 14 shows an example of a virus test result registration screen.
 ユーザは、検体および従事者に対するノロウイルス検査の検査結果を登録する場合、図3のメイン画面のウイルス検査結果登録ボタン76を押下する。これにより、図14のウイルス検査結果登録画面が表示される。 The user presses the virus test result registration button 76 on the main screen of FIG. 3 when registering the test result of the norovirus test for the sample and the worker. Thereby, the virus test result registration screen of FIG. 14 is displayed.
 ウイルス検査結果登録画面では、検体ID201および検査回数202の各項目と、検査結果入力欄203、並びに、登録ボタン204およびキャンセルボタン205が表示される。 On the virus test result registration screen, each item of the sample ID 201 and the test count 202, a test result input field 203, a registration button 204 and a cancel button 205 are displayed.
 検体ID201の項目には、ウイルス検査の検査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 201, the sample ID of the sample for which the test result of the virus test is registered is displayed. The sample ID is specified by the user.
 検査回数202の項目には、検査対象期間に指定された1週間のなかでの合計の検査回数が表示される。この例では、検査回数として「9回」が表示されており、検査対象期間に指定された1週間のなかで、製造日(ロット)を変えて、3人の従事者と検体それぞれについて3回のウイルス検査が実施されることで、合計9回の検査結果が入力される。検査対象の従事者の人数、商品の個数、一人(一個)当たりの検査回数は、図5のサンプル情報登録画面のウイルス検査ボタン134を押下して表示される設定画面で設定することができる。 In the item of the number of examinations 202, the total number of examinations in one week designated in the examination target period is displayed. In this example, “nine times” is displayed as the number of examinations, and the manufacturing date (lot) is changed within one week designated as the examination target period, and three times for each of three workers and the sample. A total of nine test results are input by performing the virus test of. The number of workers to be inspected, the number of products, and the number of inspections per person (one) can be set on the setting screen displayed by pressing the virus inspection button 134 of the sample information registration screen of FIG.
 検査結果入力欄203には、検査回数202の項目に表示されている検査回数分の結果入力欄が表示される。検査結果としては、ノロウイルスが検出された場合、陽性(+)が入力され、未検出であれば、陰性(-)が入力される。全ての検査結果が陰性(-)である場合に、問題がないと判定される。 In the inspection result input column 203, result input columns corresponding to the number of inspections displayed in the item of the number of inspections 202 are displayed. As a test result, when norovirus is detected, positive (+) is input, and negative (-) is input if it is not detected. If all test results are negative (-), it is determined that there is no problem.
 登録ボタン204は、ウイルス検査の検査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン205は、ウイルス検査の検査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 204 is pressed to register (save) after the inspection result of the virus inspection is input. The cancel button 205 is pressed to cancel the input of the inspection result of the virus inspection and to return to the main screen of FIG.
<健康管理調査結果登録画面>
 図15は、健康管理調査結果登録画面の例を示している。
<Health management survey result registration screen>
FIG. 15 shows an example of a health management survey result registration screen.
 ユーザは、個人で管理するレベルの健康管理について、従事者に調査した結果を登録する場合、図3のメイン画面の健康管理調査結果登録ボタン81を押下する。これにより、図15の健康管理調査結果登録画面が表示される。 The user presses the health management research result registration button 81 on the main screen of FIG. 3 when registering the result of surveying the worker about health management at the level managed by the individual. Thereby, the health management research result registration screen of FIG. 15 is displayed.
 健康管理調査結果登録画面では、検体ID211および調査人数212の各項目と、調査対象者切り替えボタン213、調査対象者入力欄214、調査結果入力欄215、並びに、登録ボタン216およびキャンセルボタン217が表示される。 In the health management survey result registration screen, each item of sample ID 211 and survey number of people 212, survey subject switch button 213, survey subject input column 214, survey result input column 215, registration button 216 and cancel button 217 are displayed Be done.
 検体ID211の項目には、健康管理調査の調査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 211, the sample ID of the sample for which the survey result of the health management survey is registered is displayed. The sample ID is specified by the user.
 調査人数212の項目には、検査対象期間に指定された1週間のなかで健康管理調査を行う人数が表示される。この例では、調査人数として「5人」が表示されており、この場合、検査対象期間に指定された1週間のなかで、5人の従事者に対して健康管理調査が実施される。調査人数は、図5のサンプル情報登録画面の健康管理(個人管理)ボタン141を押下して表示される設定画面で設定することができる。 In the item of the number of survey persons 212, the number of persons who carry out the health management survey within one week designated in the examination target period is displayed. In this example, “five people” are displayed as the number of persons in the survey, and in this case, a health management survey is conducted on five workers within one week designated as the examination target period. The survey number can be set on the setting screen displayed by pressing the health management (personal management) button 141 of the sample information registration screen of FIG.
 調査対象者切り替えボタン213は、調査対象者ごとに保持されている調査対象者入力欄214と調査結果入力欄215の表示を切り替えるときに押下される。図15の例では、「2人目」の調査対象者についての調査対象者入力欄214と調査結果入力欄215が表示されている。 The survey target person switching button 213 is pressed when the display of the survey target person input field 214 and the survey result input field 215 held for each survey target person is switched. In the example of FIG. 15, a survey target person input column 214 and a survey result input column 215 for the “second person” survey target are displayed.
 調査対象者入力欄214には、調査対象者の属性情報が入力される。属性情報は、例えば、会社名、所属、氏名、性別などである。 In the survey target person input field 214, attribute information of the survey target person is input. The attribute information is, for example, company name, department, name, gender and the like.
 調査結果入力欄215には、個人で管理するべき健康管理に関する各調査項目が表示される。図15の例では、「下痢をしている」、「風邪気味である、風邪を引いている」、「怪我をしている」、「手荒れや肌荒れがある」、・・・などの調査項目が表示されている。個人で管理するべき健康管理の各調査項目は、図5のサンプル情報登録画面の健康管理(個人管理)ボタン141を押下して表示される設定画面で設定することができる。ユーザは、調査結果入力欄215の該当する項目にチェックを入力する。 The survey result input field 215 displays each survey item on health management to be managed by an individual. In the example shown in FIG. 15, survey items such as "having diarrhea", "having a cold, having a cold", "having an injury", "having rough hands or rough skin", etc. Is displayed. Each survey item of health management to be managed by an individual can be set on the setting screen displayed by pressing the health management (personal management) button 141 of the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 215.
 図15は、5人の調査対象者のうちの2人目に対する1回の調査結果の例を示しているが、調査項目のうち1項目でもチェックが入力されている場合、その回の調査結果は不適と判定される。 Although FIG. 15 shows an example of one survey result for the second of five survey subjects, if a check is input even for one of the survey items, the survey result for that time is It is judged to be unsuitable.
 登録ボタン216は、健康管理についての調査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン217は、健康管理についての調査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 216 is pressed when registering (saving) after entering the survey result on health management. The cancel button 217 is pressed to cancel the input of the research result on health management and return to the main screen of FIG. 3.
<感染予防対策調査結果登録画面>
 図16は、感染予防対策調査結果登録画面の例を示している。
<Infection prevention measures findings registration screen>
FIG. 16 shows an example of the infection prevention countermeasure research result registration screen.
 ユーザは、施設の感染予防対策を調査した結果を登録する場合、図3のメイン画面の感染予防対策調査結果登録ボタン82を押下する。これにより、図16の感染予防対策調査結果登録画面が表示される。 When registering the result of investigation of infection prevention measures of the facility, the user presses the infection prevention measures research result registration button 82 on the main screen of FIG. 3. Thereby, the infection prevention countermeasure research result registration screen of FIG. 16 is displayed.
 感染予防対策調査結果登録画面では、検体ID221および調査人数222の各項目と、調査対象者切り替えボタン223、調査対象者入力欄224、調査結果入力欄225、並びに、登録ボタン226およびキャンセルボタン227が表示される。 In the infection prevention measures survey result registration screen, each item of sample ID 221 and survey number of people 222, survey target person switching button 223, survey target person input column 224, survey result input column 225, registration button 226 and cancel button 227 Is displayed.
 検体ID221の項目には、感染予防対策調査の調査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 221, the sample ID of the sample for which the investigation result of the infection prevention countermeasure investigation is registered is displayed. The sample ID is specified by the user.
 調査人数222の項目には、検査対象期間に指定された1週間のなかで感染予防対策調査を行う人数が表示される。この例では、調査人数として「5人」が表示されており、この場合、検査対象期間に指定された1週間のなかで、5人の従事者に対して感染予防対策調査が実施される。調査人数は、図5のサンプル情報登録画面の感染予防対策(施設内)ボタン142を押下して表示される設定画面で設定することができる。 In the item of the investigation number of persons 222, the number of persons who carry out the infection prevention countermeasure investigation within one week designated in the inspection target period is displayed. In this example, “five people” are displayed as the number of persons in the investigation, and in this case, an infection prevention countermeasure investigation is carried out for five workers within one week designated in the inspection target period. The number of survey persons can be set on the setting screen displayed by pressing the infection prevention countermeasure (within facility) button 142 of the sample information registration screen of FIG. 5.
 調査対象者切り替えボタン223は、調査対象者ごとに保持されている調査対象者入力欄224と調査結果入力欄225の表示を切り替えるときに押下される。図16の例では、「2人目」の調査対象者についての調査対象者入力欄224と調査結果入力欄225が表示されている。 The survey target person switching button 223 is pressed when the display of the survey target person input column 224 and the survey result input column 225 held for each survey target person is switched. In the example of FIG. 16, a survey target person input column 224 and a survey result input column 225 for the “second person” survey target are displayed.
 調査対象者入力欄224には、調査対象者の属性情報が入力される。属性情報は、例えば、会社名、所属、氏名、性別などである。 In the survey subject input column 224, attribute information of the survey subject is input. The attribute information is, for example, company name, department, name, gender and the like.
 調査結果入力欄225には、施設の感染予防対策に関する各調査項目が表示される。図16の例では、「手洗い設備が適切でない」、「汚染区域・非汚染区域が分けられていない」、「作業動線が混線している」、「材料の荷受の記録がない」、・・・などの調査項目が表示されている。感染予防対策の各調査項目は、図5のサンプル情報登録画面の感染予防対策(施設内)ボタン142を押下して表示される設定画面で設定することができる。ユーザは、調査結果入力欄225の該当する項目にチェックを入力する。 In the survey result input column 225, each survey item regarding infection prevention measures of the facility is displayed. In the example of FIG. 16, “handwashing equipment is not appropriate”, “contaminated area / non-contaminated area is not divided”, “work flow line is mixed”, “no record of receipt of material received”,・ ・ ・ ・ Investigation items such as are displayed. Each survey item of the infection prevention measures can be set on the setting screen displayed by pressing the infection prevention measures (within facility) button 142 of the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 225.
 図16は、5人の調査対象者のうちの2人目に対する1回の調査結果の例を示しているが、調査項目のうち1項目でもチェックが入力されている場合、その回の調査結果は不適と判定される。 FIG. 16 shows an example of the result of one survey for the second person out of five survey subjects, but if one of the survey items has a check input, the survey results for that time are It is judged to be unsuitable.
 登録ボタン226は、感染予防対策についての調査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン227は、感染予防対策についての調査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 226 is pressed when registering (storing) after entering the investigation result on the infection prevention measures. The cancel button 227 is pressed to cancel the input of the investigation result on the infection prevention measures and to return to the main screen of FIG. 3.
<身なり・服装・髪型・装飾調査結果登録画面>
 図17は、身なり・服装・髪型・装飾調査結果登録画面の例を示している。
<Personal appearance, clothes, hairstyle, decoration investigation result registration screen>
FIG. 17 shows an example of the appearance, clothes, hair style and decoration research result registration screen.
 ユーザは、従事者の身なり・服装・髪型・装飾について調査した結果を登録する場合、図3のメイン画面の身なり・服装・髪型・装飾調査結果登録ボタン83を押下する。これにより、図17の身なり・服装・髪型・装飾調査結果登録画面が表示される。 When registering the result of investigation on the appearance, clothes, hair style and decoration of the worker, the user presses the appearance, clothes, hair style and decoration research result registration button 83 on the main screen of FIG. As a result, the appearance, clothes, hair style and decoration research result registration screen of FIG. 17 is displayed.
 身なり・服装・髪型・装飾調査結果登録画面では、検体ID231および調査人数232の各項目と、調査対象者切り替えボタン233、調査対象者入力欄234、調査結果入力欄235、並びに、登録ボタン236およびキャンセルボタン237が表示される。 In the appearance / dress / haircut / decorative survey result registration screen, each item of the sample ID 231 and the number of survey persons 232, a survey subject switch button 233, a survey subject input column 234, a survey result input column 235, a registration button 236 and A cancel button 237 is displayed.
 検体ID231の項目には、身なり・服装・髪型・装飾調査の調査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 231, the sample ID of the sample for registering the result of the survey on appearance, clothes, hair style and decoration is displayed. The sample ID is specified by the user.
 調査人数232の項目には、検査対象期間に指定された1週間のなかで身なり・服装・髪型・装飾調査を行う人数が表示される。この例では、調査人数として「5人」が表示されており、この場合、検査対象期間に指定された1週間のなかで、5人の従事者に対して身なり・服装・髪型・装飾調査が実施される。調査人数は、図5のサンプル情報登録画面の身なり・服装・髪型・装飾ボタン143を押下して表示される設定画面で設定することができる。 In the item of the number of survey persons 232, the number of persons who carry out a survey on their appearance, clothes, hairstyles and decorations within one week designated in the examination target period is displayed. In this example, “5” is displayed as the number of persons surveyed, and in this case, surveys of appearance, clothes, hairstyles, and decorations for 5 workers are performed within one week designated as the inspection period. To be implemented. The number of persons to be surveyed can be set on the setting screen displayed by pressing the appearance / dress / hair style / decoration button 143 of the sample information registration screen of FIG. 5.
 調査対象者切り替えボタン233は、調査対象者ごとに保持されている調査対象者入力欄234と調査結果入力欄235の表示を切り替えるときに押下される。図17の例では、「2人目」の調査対象者についての調査対象者入力欄234と調査結果入力欄235が表示されている。 The survey target person switching button 233 is pressed when the display of the survey target person input column 234 and the survey result input column 235 held for each survey target person is switched. In the example of FIG. 17, a survey target person input column 234 and a survey result input column 235 for the “second” survey target person are displayed.
 調査対象者入力欄234には、調査対象者の属性情報が入力される。属性情報は、例えば、会社名、所属、氏名、性別などである。 In the survey target person input field 234, attribute information of the survey target person is input. The attribute information is, for example, company name, department, name, gender and the like.
 調査結果入力欄235には、身なり・服装・髪型・装飾に関する各調査項目が表示される。図17の例では、「毎日入力していない」、「衣服に汚れがある」、「衣服は適切に着用できていない」、「帽子・マスク・手袋をしていない」、・・・などの調査項目が表示されている。身なり・服装・髪型・装飾調査の各調査項目は、図5のサンプル情報登録画面の身なり・服装・髪型・装飾ボタン143を押下して表示される設定画面で設定することができる。ユーザは、調査結果入力欄235の該当する項目にチェックを入力する。 The survey result input field 235 displays each survey item on the appearance, clothes, hair style and decoration. In the example of FIG. 17, “Don't enter every day”, “Damage on clothes”, “Don't wear clothes properly”, “Don't wear hat, mask or gloves”, etc. Survey items are displayed. The individual survey items of the appearance, clothes, hair style and decoration investigation can be set on the setting screen displayed by pressing the appearance, clothes, hair style and decoration button 143 of the sample information registration screen of FIG. The user inputs a check in the corresponding item of the survey result input field 235.
 図17は、5人の調査対象者のうちの2人目に対する1回の調査結果の例を示しているが、調査項目のうち1項目でもチェックが入力されている場合、その回の調査結果は不適と判定される。 FIG. 17 shows an example of one survey result for the second person among the five survey subjects, but if even one of the survey items has a check input, the survey result for that time is It is judged to be unsuitable.
 登録ボタン236は、身なり・服装・髪型・装飾についての調査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン237は、身なり・服装・髪型・装飾についての調査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 236 is pressed in the case of registration (storage) after the search results on the appearance, clothes, hairstyle and decoration are input. The cancel button 237 is pressed to cancel the input of the research result on the appearance, clothes, hairstyle and decoration and to return to the main screen of FIG.
<衛生教育調査結果登録画面>
 図18は、衛生教育調査結果登録画面の例を示している。
<Satellite education findings registration screen>
FIG. 18 shows an example of the hygiene education research result registration screen.
 ユーザは、衛生教育の体制や従事者の理解度についての調査結果を登録する場合、図3のメイン画面の衛生教育調査結果登録ボタン84を押下する。これにより、図18の衛生教育調査結果登録画面が表示される。 The user presses the hygiene education survey result registration button 84 on the main screen of FIG. 3 when registering the survey result on the health education system and the degree of understanding of the worker. Thereby, the hygiene education research result registration screen of FIG. 18 is displayed.
 衛生教育調査結果登録画面では、検体ID241および調査人数242の各項目と、調査対象者切り替えボタン243、調査対象者入力欄244、調査結果入力欄245、並びに、登録ボタン246およびキャンセルボタン247が表示される。 In the hygiene education survey result registration screen, each item of sample ID 241 and survey number of people 242, survey target person switching button 243, survey target person input column 244, survey result input column 245, registration button 246 and cancel button 247 are displayed Be done.
 検体ID241の項目には、衛生教育についての調査結果を登録する検体の検体IDが表示される。この検体IDは、ユーザによって指定される。 In the item of the sample ID 241, the sample ID of the sample for which the survey result on the hygiene education is registered is displayed. The sample ID is specified by the user.
 調査人数242の項目には、検査対象期間に指定された1週間のなかで衛生教育についての調査を行う人数が表示される。この例では、調査人数として「5人」が表示されており、この場合、検査対象期間に指定された1週間のなかで、5人の従事者に対して衛生教育についての調査が実施される。調査人数は、図5のサンプル情報登録画面の衛生教育(知識)ボタン144を押下して表示される設定画面で設定することができる。 In the item of the number of survey persons 242, the number of persons who conduct surveys on hygiene education within one week designated as the inspection target period is displayed. In this example, "5" is displayed as the number of surveys, and in this case, a survey on hygiene education is conducted for 5 workers within one week specified in the inspection period. . The number of persons surveyed can be set on the setting screen displayed by pressing the hygiene education (knowledge) button 144 of the sample information registration screen of FIG. 5.
 調査対象者切り替えボタン243は、調査対象者ごとに保持されている調査対象者入力欄244と調査結果入力欄245の表示を切り替えるときに押下される。図18の例では、「2人目」の調査対象者についての調査対象者入力欄244と調査結果入力欄245が表示されている。 The survey target person switching button 243 is pressed when the display of the survey target person input field 244 and the survey result input field 245 held for each survey target person is switched. In the example of FIG. 18, a survey target person input column 244 and a survey result input column 245 for the “second” survey target person are displayed.
 調査対象者入力欄244には、調査対象者の属性情報が入力される。属性情報は、例えば、会社名、所属、氏名、性別などである。 In the survey subject input column 244, attribute information of the survey subject is input. The attribute information is, for example, company name, department, name, gender and the like.
 調査結果入力欄245には、衛生教育に関する各調査項目が表示される。図18の例では、「月1度の検便検査を実施していない(頻度)」、「検便検査は全員が実施していない(対象者)」、「食中毒細菌の怖さを知らない」、「正しい手洗いの仕方を知らない」、・・・などの調査項目が表示されている。衛生教育についての各調査項目は、図5のサンプル情報登録画面の衛生教育(知識)ボタン144を押下して表示される設定画面で設定することができる。ユーザは、調査結果入力欄245の該当する項目にチェックを入力する。 In the survey result input field 245, each survey item related to hygiene education is displayed. In the example of FIG. 18, “monthly stool examination is not performed (frequency)”, “all stool examinations are not performed (subject)”, “we do not know fear of food poisoning bacteria”, Survey items such as "I do not know how to wash my hands" are displayed. Each survey item on hygiene education can be set on the setting screen displayed by pressing the hygiene education (knowledge) button 144 on the sample information registration screen of FIG. 5. The user inputs a check in the corresponding item of the survey result input field 245.
 図18は、5人の調査対象者のうちの2人目に対する1回の調査結果の例を示しているが、調査項目のうち1項目でもチェックが入力されている場合、その回の調査結果は不適と判定される。 FIG. 18 shows an example of the result of one survey for the second person among the five survey subjects, but if one of the survey items has a check input, the survey results for that time are It is judged to be unsuitable.
 登録ボタン246は、衛生教育についての調査結果を入力後、登録(保存)する場合に押下される。キャンセルボタン247は、衛生教育についての調査結果の入力をキャンセルし、図3のメイン画面に戻る場合に押下される。 The registration button 246 is pressed in the case of registration (storage) after inputting the survey result on hygiene education. A cancel button 247 is pressed to cancel the input of the survey result on hygiene education and return to the main screen of FIG. 3.
<結果一覧画面>
 図19は、結果一覧画面の例を示している。
<Result list screen>
FIG. 19 shows an example of the result list screen.
 ユーザは、検体の各検査項目の結果の一覧を表示させる際に、図3のメイン画面の結果一覧ボタン91を押下する。これにより、図19の結果一覧画面が表示される。 The user presses the result list button 91 of the main screen of FIG. 3 when displaying the list of the results of each test item of the sample. Thereby, the result list screen of FIG. 19 is displayed.
 結果一覧画面では、顧客名251、施設名252、施設CD253、サブCD254、検体名255、検体ID256、検査結果表示欄257、調査日258、及び調査者259の各項目と、閉じるボタン260が表示される。 In the result list screen, each item of customer name 251, facility name 252, facility CD 253, sub CD 254, sample name 255, sample ID 256, test result display column 257, survey date 258, and surveyor 259, and close button 260 are displayed. Be done.
 結果一覧画面の顧客名251、施設名252、施設CD253、及びサブCD254の各項目には、サンプル情報登録画面の顧客名121、施設名122、施設CD123、及びサブCD124と同様に、顧客の会社名及び施設名と、そのコード番号(CD)が表示される。 The customer name 251, the facility name 252, the facility CD 253, and the sub CD 254 in the result list screen include the customer name 121, the facility name 122, the facility CD 123, and the sub CD 124 of the sample information registration screen. The name and facility name and its code number (CD) are displayed.
 ただし、顧客名251と施設名252には、それぞれ、検索ボタン251Aと252Aが付加されている。顧客名251には、ユーザが検索ボタン251Aを押下することにより表示された顧客リストから選択された顧客の会社名が表示される。同様に、施設名252には、ユーザが検索ボタン252Aを押下することにより表示された施設名リストから選択された施設名が表示される。 However, search buttons 251A and 252A are added to the customer name 251 and the facility name 252, respectively. In the customer name 251, the company name of the customer selected from the customer list displayed by the user pressing the search button 251A is displayed. Similarly, in the facility name 252, the facility name selected from the facility name list displayed by the user pressing the search button 252A is displayed.
 検体名255及び検体ID256には、サンプル情報登録画面の検体名125及び検体ID126と同様に、検査した対象の食品の名前、及び、検体IDが表示される。 In the sample name 255 and the sample ID 256, similarly to the sample name 125 and the sample ID 126 on the sample information registration screen, the name of the inspected food and the sample ID are displayed.
 検体名255と検体ID256にも、それぞれ、検索ボタン255Aと256Aが付加されている。検体名255には、検索ボタン255Aを押下することにより表示された検体リストから選択された商品名が表示される。検体ID256には、検索ボタン256Aを押下することにより表示された検体IDリストから選択された検体IDが表示される。 Search buttons 255A and 256A are added to the sample name 255 and the sample ID 256, respectively. As the sample name 255, a product name selected from the sample list displayed by pressing the search button 255A is displayed. In the sample ID 256, the sample ID selected from the sample ID list displayed by pressing the search button 256A is displayed.
 検査結果表示欄257には、検体ID256に表示された検体IDで識別される検体について、これまで検査が終了している範囲内で、検査結果が表示される。検査結果表示欄257のスペースよりも表示項目が多い場合には、スクロールすることで、非表示の検査結果を表示させることができる。 In the test result display column 257, test results are displayed for the sample identified by the sample ID displayed in the sample ID 256 within the range in which the test has been completed. When there are more display items than the space of the test result display column 257, the non-displayed test results can be displayed by scrolling.
 調査日258の項目には、検体ID256に表示された検体IDで識別される検体について、検査および調査した日付が表示される。検査および調査した日付が複数存在する場合には、例えば、最終(直近)の日付が表示される。 In the item of the investigation date 258, the date on which the examination and investigation were performed on the sample identified by the sample ID displayed in the sample ID 256 is displayed. In the case where there are a plurality of dates checked and examined, for example, the last (last) date is displayed.
 調査者259の項目には、検体ID256に表示された検体IDで識別される検体について調査した担当者の名前が表示される。 In the item of the researcher 259, the names of persons in charge who have investigated the sample identified by the sample ID displayed in the sample ID 256 are displayed.
 閉じるボタン260は、結果一覧画面の表示を終了し、図3のメイン画面に戻る場合に押下される。 The close button 260 is pressed when ending the display of the result list screen and returning to the main screen of FIG. 3.
<結果出力画面>
 図20は、結果出力画面の例を示している。
<Result output screen>
FIG. 20 shows an example of the result output screen.
 ユーザは、検体についての検査結果および調査結果に基づく最終的な安全度の判定結果を表示させる際に、図3のメイン画面の結果出力ボタン92を押下する。これにより、図20の結果出力画面が表示される。 The user presses the result output button 92 on the main screen of FIG. 3 when displaying the final determination result of the degree of safety based on the inspection result and the inspection result of the sample. Thereby, the result output screen of FIG. 20 is displayed.
 結果出力画面では、顧客名271、施設名272、施設CD273、サブCD274、検体名275、検体ID276、及びスケール判定結果表示欄277の各項目と、閉じるボタン278及び証明書発行ボタン279が表示される。 On the result output screen, each item of the customer name 271, the facility name 272, the facility CD 273, the sub CD 274, the sample name 275, the sample ID 276, and the scale determination result display field 277, the close button 278 and the certificate issuance button 279 are displayed. Ru.
 顧客名271、施設名272、施設CD273、サブCD274、検体名275、及び検体ID276は、図19の結果一覧画面の顧客名251、施設名252、施設CD253、サブCD254、検体名255、及び検体ID256と、それぞれ同様である。顧客名271、施設名272、検体名275、及び検体ID276にも、それぞれ、検索ボタン271A、272A、275A、及び276Aが付加されている。 The customer name 271, the facility name 272, the facility CD 273, the sub CD 274, the sample name 275, and the sample ID 276 are the customer name 251, the facility name 252, the facility CD 253, the sub CD 254, the sample name 255, and the sample of the result list screen in FIG. The same as ID 256, respectively. Search buttons 271A, 272A, 275A, and 276A are also added to the customer name 271, the facility name 272, the sample name 275, and the sample ID 276, respectively.
 スケール判定結果表示欄277には、検体ID256に表示された検体IDで識別される検体についての検査結果および調査結果に基づいて、安全度算出部106により算出された健康被害に対する安全度が、判定結果として表示される。 In the scale determination result display field 277, the safety degree for the health damage calculated by the safety degree calculation unit 106 is determined based on the examination result and the examination result for the sample identified by the sample ID displayed in the sample ID 256 Displayed as a result.
 スケール判定結果表示欄277に表示される安全度は、指数形式の値で表される。安全度算出部106により算出される安全度には、安全度の大きさに応じて割り当てられている色が存在する。 The degree of safety displayed in the scale determination result display field 277 is represented by a value in the exponential format. The safety degree calculated by the safety degree calculation unit 106 includes a color assigned according to the magnitude of the safety degree.
 スケール判定結果表示欄277には、安全度の大きさに応じて割り当てられている色の見本である安全度色見本スケール277Aとともに、結果表示部277Bに、安全度算出部106により算出された検体の安全度「3.7×10-9」と、それに対応する色である所定のグレイ色が表示されている。安全度算出部106による安全度の算出方法については後述する。ユーザは、10のべき乗で表される安全度の指数部分の値「-9」および安全度に対応する色によって、検体の安全度を一目で把握することができる。 In the scale determination result display column 277, the sample calculated by the safety degree calculation unit 106 in the result display unit 277B together with the safety degree color sample scale 277A which is a sample of the color assigned according to the size of the safety degree And a predetermined gray color which is a color corresponding to the degree of safety “3.7 × 10 −9 ”. The calculation method of the safety degree by the safety degree calculation unit 106 will be described later. The user can grasp the degree of safety of the sample at a glance by the value "-9" of the exponent part of the degree of safety expressed by a power of 10 and the color corresponding to the degree of safety.
 図20では、モノクロ表示の制約があるため、安全度色見本スケール277Aは、安全度の大きさに応じて、黒から白までの濃淡で表されているが、カラー表示が可能な画面では、例えば、安全度の大きさに応じて、10-2付近が青色の寒色系、10-10付近が赤色の暖色系となるような、可視光線の波長に対応するカラー色が割り当てられて表示されている。 In FIG. 20, there is a restriction on monochrome display, so the safety degree color sample scale 277A is represented by the shade from black to white according to the magnitude of the safety degree, but on a screen where color display is possible, For example, according to the degree of safety, a color corresponding to the wavelength of visible light is assigned and displayed such that a cold color system in the vicinity of 10 -2 becomes a warm color system in the vicinity of 10 -2 and a red color around 10 -10. ing.
 閉じるボタン278は、結果出力画面の表示を終了し、図3のメイン画面に戻る場合に押下される。 The close button 278 is pressed when ending the display of the result output screen and returning to the main screen of FIG. 3.
 証明書発行ボタン279は、検体の安全度の検査証明書を発行する場合に押下される。証明書発行ボタン279が押下された場合、図21に示すような検査証明書が印刷される。 The certificate issuance button 279 is pressed when issuing a test certificate of the degree of safety of the sample. When the certificate issuance button 279 is pressed, an inspection certificate as shown in FIG. 21 is printed.
 図21の検査証明書では、安全度算出部106により算出された検体の安全度の指数部分の値「-9」が、大きなサイズで表示されるとともに、安全度に対応するグレイ色(カラー色)を使用したマーク(星)が付されている。ここで表示される検体の安全度の指数部分の値「-9」及びグレイ色は、図20の結果表示部277Bに表示されている安全度の値及びグレイ色と同一である。 In the examination certificate of FIG. 21, the value “-9” of the index portion of the safety degree of the sample calculated by the safety degree calculation unit 106 is displayed in a large size, and the gray color (color color corresponding to the safety degree The mark (star) is attached using). The value “−9” and the gray color of the exponent part of the degree of safety of the sample displayed here are the same as the value of the degree of safety and the gray color displayed in the result display portion 277B of FIG.
<安全度の算出方法>
 次に、安全度算出部106による検体の安全度の算出方法について説明する。
<How to calculate the degree of safety>
Next, a method of calculating the degree of safety of the sample by the degree of safety calculation unit 106 will be described.
 以下では、図6乃至図18に示した検査結果および調査結果の例を用いて、安全度の算出方法について説明する。 In the following, the method of calculating the degree of safety will be described using the examples of the inspection results and the investigation results shown in FIGS. 6 to 18.
 安全度の算出処理では、初めに、メイン画面からユーザによって入力された検体の検査結果及び調査結果に基づいて、検体のリスク(危険度)の大きさが算出される。そして、健康被害に対する検体の安全度は、算出されたリスク(危険度)の大きさの裏返しであるとの考えから、算出されたリスクの大きさの逆数で与えられると定義する。 In the process of calculating the degree of safety, first, the magnitude of the risk (the degree of risk) of the sample is calculated based on the examination result and the examination result of the sample input by the user from the main screen. And, it is defined that the safety level of the sample for the health hazard is given by the reciprocal of the calculated magnitude of the risk, considering that it is the reverse of the magnitude of the calculated risk (risk level).
 そこで、初めに、図6乃至図18に示した検査結果および調査結果から、検体のリスク(危険度)の大きさの算出方法について説明する。 Therefore, first, from the test results and the survey results shown in FIGS. 6 to 18, a method of calculating the magnitude of the risk (risk degree) of the sample will be described.
 検体のリスクの大きさは、検査結果登録グループに属する各検査項目と、調査結果登録グループに属する各調査項目のそれぞれについて算出されたリスクの大きさの積で表される。そして、検査結果登録グループに属する各検査項目と、調査結果登録グループに属する各調査項目のそれぞれのリスクの大きさは、リスクの影響度とリスク発生頻度の積、すなわち、「所定の検査・調査項目のリスクの大きさ = リスクの影響度 × リスクの発生頻度」で定義される。 The magnitude of the risk of the sample is represented by the product of the magnitude of the risk calculated for each examination item belonging to the examination result registration group and each examination item belonging to the investigation result registration group. Then, the magnitude of the risk of each inspection item belonging to the inspection result registration group and each inspection item belonging to the investigation result registration group is the product of the risk impact degree and the risk occurrence frequency, that is, “predetermined inspection / inspection It is defined by “Risk of item = Risk impact × Frequency of occurrence of risk”.
 リスクの影響度は、リスク影響度判定部104により、例えば、n(n>1)段階で判定される。例えば、リスクの影響度を5段階で判定するとした場合、「5:人の死に直結するレベル、4:人の死の可能性あり、3:担当者レベルの危機、2:やや影響がある、1:ほとんど影響がない」という基準に即して、各検査・調査項目のリスクの影響度が、図22に示すように予め設定される。 The risk influence degree is determined by the risk influence degree determination unit 104, for example, in n (n> 1) stages. For example, if it is judged that the degree of influence of risk is in five stages, "5: level directly linked to human death, 4: possible human death, 3: crisis at representative level, 2: slightly affected, 1: In accordance with the standard that “there is almost no effect”, the degree of risk influence of each inspection / study item is preset as shown in FIG.
 農薬・抗生物質、放射線測定、および、アレルゲン混入の検査結果については、「5:基準値以上の項目がある場合、4:基準値以下の値が20%以上の項目で検出されている場合、3:基準値以下の値が10%以上20%未満の項目で検出されている場合、2:基準値以下の値が10%未満の項目で検出されている場合、1:全て未検出(検出不可レベル)」のように、影響度が設定されている。 For the test results of pesticides / antibiotics, radiation measurement, and allergen contamination, “5: When there is an item above the standard value, 4: When the value below the standard value is detected by an item of 20% or more, 3: When the value below the reference value is detected in the item of 10% or more and less than 20%, 2: When the value below the reference value is detected in the item of less than 10% 1: All not detected (detection The impact level is set as "impossible level)".
 食中毒細菌(毒素)およびウイルス検査の検査結果については、1つでも毒素が検出されると重大な問題であるので、毒素が検出された場合の影響度「5」と、一つも検出されなかった場合の影響度「1」のみが設定されている。 As for the test result of food poisoning bacteria (toxin) and virus test, even if one is a serious problem if the toxin is detected, the influence "5" when the toxin is detected, one is not detected either Only the influence degree "1" of the case is set.
 異物混入の検査結果については、「5:毎日起こるレベルである場合、4:毎週起こるレベルである場合、3:毎月起こるレベルである場合、2:数か月に1回起こるレベルである場合、1:半年以上発生していない場合」のように、影響度が設定されている。 Regarding the inspection result of the contamination, “5: When the level occurs every day, 4: when the level occurs every week, 3: when the level occurs every month, 2: when the level occurs once every several months, The degree of influence is set as “1: no occurrence for more than half a year”.
 調査結果登録グループの各調査項目については、「5:不適者が5人いる場合、4:不適者が4人いる場合、3:不適者が3人いる場合、2:不適者が2人いる場合、1:不適者が1以下である場合」のように、影響度が設定されている。 For each survey item in the survey result registration group, “5: If there are 5 unqualified persons, 4: If there are 4 inadequate persons, 3: If there are 3 inadequate persons, 2: If there are 2 inadequate persons In the case 1: the case where the unfit person is 1 or less, the degree of influence is set.
 図6乃至図18に示した検査結果および調査結果を参照して、各検査項目および各調査項目におけるリスクの大きさの算出について順番に説明する。 Calculation of the magnitude of the risk in each inspection item and each investigation item will be described in order with reference to the inspection results and the investigation results shown in FIGS. 6 to 18.
 初めに、食中毒細菌(毒素)のリスクの大きさの算出について説明する。 First, the calculation of the magnitude of the risk of food poisoning bacteria (toxins) will be described.
 食中毒細菌(毒素)のリスクの影響度は、図22に示したように、1つでも毒素が検出されると重大な問題であるので、1つでも毒素が検出された場合は影響度「5」、一つも検出されなかった場合は影響度「1」に設定される。 The degree of risk of food poisoning bacteria (toxins) is a serious problem if even one toxin is detected, as shown in FIG. If no one is detected, the degree of influence is set to "1".
 また、食中毒細菌(毒素)のリスクの発生頻度は、リスクの影響度と同じ値に設定される。すなわち、1つでも毒素が検出された場合は発生頻度「5」、一つも検出されなかった場合は発生頻度「1」に設定される。 In addition, the frequency of risk of food poisoning bacteria (toxins) is set to the same value as the risk impact. That is, the occurrence frequency is set to "5" when at least one toxin is detected, and the occurrence frequency "1" when no toxin is detected.
 図6の食中毒細菌検査結果登録画面で入力された検査結果では、2回目の検査で大腸菌群、3回目の検査で、大腸菌群、カビ、および酵母、4回目の検査で、大腸菌群、カビ、および、黄色ブドウ球菌が検出されている。この場合、リスク影響度判定部104は、リスクの影響度を「5」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「5」と判定する。したがって、安全度算出部106により算出される食中毒細菌(毒素)のリスクの大きさは、5×5=25となる。 In the test results entered on the food poisoning bacteria test result registration screen of FIG. 6, the coliform group in the second test, coliform group, mold, and yeast in the third test, coliform group, mold in the fourth test, And, S. aureus has been detected. In this case, the risk impact determination unit 104 determines that the risk impact is “5”, and the risk occurrence frequency determination unit 105 determines that the risk occurrence frequency is “5”. Therefore, the magnitude of the risk of food poisoning bacteria (toxin) calculated by the safety degree calculation unit 106 is 5 × 5 = 25.
 次に、農薬・抗生物質のリスクの大きさの算出について説明する。 Next, the calculation of the magnitude of the risk of pesticides and antibiotics will be explained.
 農薬・抗生物質のリスクの影響度は、図22に示したように、「5:基準値以上の項目がある場合、4:基準値以下の値が20%以上の項目で検出されている場合、3:基準値以下の値が10%以上20%未満の項目で検出されている場合、2:基準値以下の値が10%未満の項目で検出されている場合、1:全て未検出」のように設定される。 As shown in FIG. 22, “5: When there is an item above the reference value, 4: When the value below the reference value is detected in the item above 20%, as shown in FIG. 3: When the value below the reference value is detected in the item of 10% or more and less than 20% 2: When the value below the reference value is detected in the item of less than 10% 1: All not detected It is set as
 また、農薬・抗生物質のリスクの発生頻度は、リスクの影響度と同じ値に設定される。 In addition, the frequency of occurrence of risks for pesticides and antibiotics is set to the same value as the risk impact.
 図7の農薬・抗生物質検査結果登録画面で入力された検査結果では、「4-クロルフェノキシ酢酸(4-CPA)」について基準値以上の値が検出されている。この場合、リスク影響度判定部104は、リスクの影響度を「5」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「5」と判定する。したがって、安全度算出部106により算出される農薬・抗生物質のリスクの大きさは、5×5=25となる。 In the test results input on the agrochemical / antibiotic test result registration screen of FIG. 7, a value equal to or higher than the reference value is detected for “4-chlorophenoxyacetic acid (4-CPA)”. In this case, the risk impact determination unit 104 determines that the risk impact is “5”, and the risk occurrence frequency determination unit 105 determines that the risk occurrence frequency is “5”. Therefore, the magnitude of the risk of the pesticide / antibiotics calculated by the safety degree calculation unit 106 is 5 × 5 = 25.
 次に、放射線測定のリスクの大きさの算出について説明する。 Next, calculation of the magnitude of the risk of radiation measurement will be described.
 放射線測定のリスクの影響度は、図22に示したように、「5:基準値以上の項目がある場合、4:基準値以下の値が20%以上の項目で検出されている場合、3:基準値以下の値が10%以上20%未満の項目で検出されている場合、2:基準値以下の値が10%未満の項目で検出されている場合、1:全て未検出」のように設定される。 As shown in FIG. 22, “5: When there is an item above the reference value, 4: When the value below the reference value is detected by an item of 20% or more, as shown in FIG. : When the value below the reference value is detected in the item of 10% or more and less than 20%, 2: When the value below the reference value is detected in the item of less than 10%, 1: All not detected Set to
 放射線測定のリスクの発生頻度には、全て未検出(基準値未満)の場合は、最小値である「1」が設定され、1回以上検出された場合は、その検出回数が設定される。 The occurrence frequency of risk of radiation measurement is set to “1” which is the minimum value in the case of all undetected (less than the reference value), and the number of times of detection is set in the case of one or more detections.
 図11の放射線測定結果登録画面で入力された検査結果では、3回全ての検査において、未検出であるので、リスク影響度判定部104は、リスクの影響度を「1」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「1」と判定する。したがって、安全度算出部106により算出される放射線測定のリスクの大きさは、1×1=1となる。 In the inspection result input on the radiation measurement result registration screen of FIG. 11, the risk influence degree determination unit 104 determines the degree of influence of the risk as “1” because the detection result is not detected in all the three examinations. The occurrence frequency determination unit 105 determines that the risk occurrence frequency is “1”. Therefore, the magnitude of the risk of radiation measurement calculated by the safety degree calculation unit 106 is 1 × 1 = 1.
 次に、異物混入のリスクの大きさの算出について説明する。 Next, calculation of the magnitude of the risk of contamination will be described.
 異物混入のリスクの影響度は、図22に示したように、「5:毎日起こるレベルである場合、4:毎週起こるレベルである場合、3:毎月起こるレベルである場合、2:数か月に1回起こるレベルである場合、1:半年以上発生していない場合」のように設定される。 As shown in FIG. 22, the influence level of the risk of foreign body contamination is “5: when the level occurs daily, 4: when the level occurs weekly, 3: when the level occurs monthly, 2: several months If it is a level that occurs once, it is set as “1: when it has not occurred for more than half a year”.
 異物混入のリスクの発生頻度には、「X線検出器」、「個人装備」、「外気汚染」、「昆虫飛来」、「防鼠対策」、「設備老朽具合」、「清掃頻度」、「改善チームの有無」、及び「製品保存状態」の各検査項目のうち、[NG]と判定された検査項目の個数が設定される。 The frequency of occurrence of the risk of contamination is “X-ray detector”, “personal equipment”, “open air pollution”, “insect flying”, “anti-corrosion measures”, “equipment condition”, “cleaning frequency”, “ The number of inspection items determined as “NG” is set among the inspection items “presence of improvement team” and “product storage state”.
 図12の異物混入検査結果登録画面で入力された検査結果では、発生頻度入力欄184で、発生頻度が「毎日起こるレベルである」と入力されており、検査結果入力欄183では、「X線検出器」、「個人装備」、「外気汚染」、及び「昆虫飛来」の4項目で、[NG]と判定されている。したがって、リスク影響度判定部104は、リスクの影響度を「5」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「4」と判定する。これにより、安全度算出部106により算出される異物混入のリスクの大きさは、5×4=20となる。 In the inspection result input on the foreign substance contamination inspection result registration screen of FIG. 12, the occurrence frequency is input in the occurrence frequency input field 184 as “everyday is a level”, and in the inspection result entry field 183, “X-ray” It is judged as [NG] by four items of "detector", "personal equipment", "air pollution", and "insect flying". Therefore, the risk impact determination unit 104 determines that the risk impact is “5”, and the risk occurrence frequency determination unit 105 determines that the risk occurrence frequency is “4”. Thereby, the magnitude of the risk of foreign matter mixing calculated by the safety degree calculation unit 106 is 5 × 4 = 20.
 次に、アレルゲン混入のリスクの大きさの算出について説明する。 Next, calculation of the magnitude of the risk of allergen contamination will be described.
 アレルゲン混入のリスクの影響度は、図22に示したように、「5:基準値以上の項目がある場合、4:基準値以下の値が20%以上の項目で検出されている場合、3:基準値以下の値が10%以上20%未満の項目で検出されている場合、2:基準値以下の値が10%未満の項目で検出されている場合、1:全て未検出」のように設定される。 As shown in FIG. 22, “5: when there is an item above the reference value, 4: when the value below the reference value is detected in the item of 20% or more, as shown in FIG. : When the value below the reference value is detected in the item of 10% or more and less than 20%, 2: When the value below the reference value is detected in the item of less than 10%, 1: All not detected Set to
 アレルゲン混入のリスクの発生頻度には、全て未検出の場合は、最小値である「1」が設定され、1回以上検出された場合は、その検出回数が設定される。 The occurrence frequency of the risk of mixing with the allergen is set to “1” which is the minimum value if not all detected, and the number of times of detection is set if detected once or more.
 図13のアレルゲン混入検査結果登録画面で入力された検査結果では、3回のアレルゲン混入検査のうち、2回の検査で所定のアレルゲンが検出されているので、リスク影響度判定部104は、リスクの影響度を「5」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「2」と判定する。したがって、安全度算出部106により算出されるアレルゲン混入のリスクの大きさは、5×2=10となる。 In the test result input on the allergen contamination test result registration screen of FIG. 13, a predetermined allergen is detected in two of the three allergen contamination tests, so the risk influence degree determination unit 104 The risk occurrence frequency determination unit 105 determines that the risk occurrence frequency is “2”. Therefore, the magnitude of the risk of contamination with the allergen calculated by the safety degree calculation unit 106 is 5 × 2 = 10.
 次に、ウイルス検査のリスクの大きさの算出について説明する。 Next, calculation of the magnitude of the risk of virus testing will be described.
 ウイルス検査のリスクの影響度は、図22に示したように、1つでも毒素が検出されると重大な問題であるので、1つでも毒素が検出された場合は影響度「5」、一つも検出されなかった場合は影響度「1」に設定される。 As shown in FIG. 22, the degree of influence of the risk of virus testing is a serious problem if even one toxin is detected, the degree of influence “5” if one toxin is detected, one If one is not detected, the degree of influence is set to "1".
 ウイルス検査のリスクの発生頻度には、全て未検出の場合は、最小値である「1」が設定され、1回以上検出された場合は、その検出回数が設定される。 The occurrence frequency of the risk of virus inspection is set to “1” which is the minimum value if not all detected, and the number of times of detection is set if detected once or more.
 図14のウイルス検査結果登録画面で入力された検査結果では、9回の検査のうち、3回の検査でノロウイルスが検出されているので、リスク影響度判定部104は、リスクの影響度を「5」と判定し、リスク発生頻度判定部105は、リスクの発生頻度を「3」と判定する。したがって、安全度算出部106により算出される放射線測定のリスクの大きさは、5×3=15となる。 In the test result input on the virus test result registration screen of FIG. 14, since the norovirus is detected in three tests out of nine tests, the risk influence determination unit 104 determines that the risk influence degree The risk occurrence frequency determination unit 105 determines that the risk occurrence frequency is “3”. Therefore, the magnitude of the risk of radiation measurement calculated by the safety degree calculation unit 106 is 5 × 3 = 15.
 次に、健康管理のリスクの大きさの算出について説明する。 Next, the calculation of the magnitude of health management risk will be described.
 健康管理のリスクの影響度は、「5:不適者が5人いる場合、4:不適者が4人いる場合、3:不適者が3人いる場合、2:不適者が2人いる場合、1:不適者が1以下である場合」のように設定される。 The impact of health management risk is as follows: "5: If there are 5 unfit people, 4: If there are 4 unfit people, 3: If there are 3 unfit people, 2: If there are 2 unfit people, 1: It is set as "when the unsuitable person is 1 or less".
 健康管理のリスクの発生頻度には、不適と判定された調査回数の合計が設定される。 The frequency of health care risk occurrence is set to the sum of the number of surveys judged to be unsuitable.
 図15の健康管理調査結果登録画面の例は、5人の調査対象者のうちの2人目に対する1回の調査結果であるが、5人の調査対象者のうちの3人に対して、不適と判定された調査結果が1回ずつ登録されているとする。この場合、リスク影響度判定部104は、不適者が3人であるので、リスクの影響度を「3」と判定し、リスク発生頻度判定部105は、3人が1回ずつで計3回不適と判定されているので、リスクの発生頻度を「3」と判定する。したがって、安全度算出部106により算出される放射線測定のリスクの大きさは、3×3=9となる。 The example of the health management survey result registration screen in FIG. 15 is one survey result for the second one of the five survey subjects, but is unsuitable for three of the five survey subjects. It is assumed that the survey results determined to have been registered one by one. In this case, since the risk impact determination unit 104 determines that the risk impact is “3” because there are three unqualified persons, the risk occurrence frequency determination unit 105 is performed three times in each of the three occurrences. Since the risk is determined to be inappropriate, the risk occurrence frequency is determined to be "3". Therefore, the magnitude of the risk of radiation measurement calculated by the safety degree calculation unit 106 is 3 × 3 = 9.
 感染予防対策のリスクの大きさの算出について説明する。 Explain the calculation of the risk of infection prevention measures.
 感染予防対策のリスクの影響度は、「5:不適者が5人いる場合、4:不適者が4人いる場合、3:不適者が3人いる場合、2:不適者が2人いる場合、1:不適者が1以下である場合」のように設定される。 The impact of the infection prevention measures is "5: If there are 5 unfit people, 4: If there are 4 unfit people, 3: If there are 3 unfit people, 2: If there are 2 unfit people , 1: when the unsuitable person is 1 or less. "
 感染予防対策のリスクの発生頻度には、不適と判定された調査回数の合計が設定される。 The frequency of risk of infection control measures is set to the total number of surveys judged to be unsuitable.
 図16の感染予防対策調査結果登録画面の例は、5人の調査対象者のうちの2人目に対する1回の調査結果であるが、5人の調査対象者のうちの2人に対して、不適と判定された調査結果が1回ずつ登録されているとする。この場合、リスク影響度判定部104は、不適者が2人であるので、リスクの影響度を「2」と判定し、リスク発生頻度判定部105は、2人が1回ずつで計2回不適と判定されているので、リスクの発生頻度を「2」と判定する。したがって、安全度算出部106により算出される感染予防対策のリスクの大きさは、2×2=4となる。 The example of the infection prevention measures survey result registration screen in FIG. 16 is one survey result for the second of five survey subjects, but for two of the five survey subjects, It is assumed that the survey results determined to be unsuitable are registered one by one. In this case, the risk impact determination unit 104 determines that the risk impact is “2” because there are two unqualified persons, and the risk occurrence frequency determination unit 105 is performed twice by two people each. Since the risk is determined to be inappropriate, the risk occurrence frequency is determined to be "2". Therefore, the magnitude of the risk of infection prevention measures calculated by the safety degree calculation unit 106 is 2 × 2 = 4.
 身なり・服装・髪型・装飾のリスクの大きさの算出について説明する。 Explain the calculation of the size of the risk of wear, clothes, hairstyle and decoration.
 身なり・服装・髪型・装飾のリスクの影響度は、「5:不適者が5人いる場合、4:不適者が4人いる場合、3:不適者が3人いる場合、2:不適者が2人いる場合、1:不適者が1以下である場合」のように設定される。 The impact of the risk of appearance, clothes, hairstyle and decoration is as follows: "5: If there are 5 unfit people, 4: If there are 4 unfit people, 3: If there are 3 unfit people, 2: If the unfit people are When there are two people, it is set as “1: Inadequate person is 1 or less”.
 身なり・服装・髪型・装飾のリスクの発生頻度には、不適と判定された調査回数の合計が設定される。 The frequency of the risk of appearance, clothes, hairstyle and decoration is set to the sum of the number of surveys judged to be unsuitable.
 図17の身なり・服装・髪型・装飾調査結果登録画面の例は、5人の調査対象者のうちの2人目に対する1回の調査結果であるが、5人の調査対象者のうちの1人に対して、不適と判定された調査結果が1回だけ登録されているとする。この場合、リスク影響度判定部104は、不適者が1人であるので、リスクの影響度を「1」と判定し、リスク発生頻度判定部105は、1人が1回で計1回不適と判定されているので、リスクの発生頻度を「1」と判定する。したがって、安全度算出部106により算出される、身なり・服装・髪型・装飾のリスクの大きさは、1×1=1となる。 The example of the appearance / dress / haircut / decoration research result registration screen shown in FIG. 17 is one survey result for the second of five persons to be surveyed, but one of five persons to be surveyed On the other hand, it is assumed that the survey result judged to be unsuitable is registered only once. In this case, the risk impact determination unit 104 determines that the risk impact is “1” because the number of inappropriate persons is one, and the risk occurrence frequency determination unit 105 is inappropriate once for one person. Since it is determined that the risk occurrence frequency is "1". Therefore, the size of the risk of wear, clothes, hairstyle and decoration calculated by the safety degree calculation unit 106 is 1 × 1 = 1.
 衛生教育のリスクの大きさの算出について説明する。 Explain the calculation of the magnitude of the risk of hygiene education.
 衛生教育のリスクの影響度は、「5:不適者が5人いる場合、4:不適者が4人いる場合、3:不適者が3人いる場合、2:不適者が2人いる場合、1:不適者が1以下である場合」のように設定される。 The influence level of the risk of hygiene education is "5: When there are 5 unfit people, 4: When there are 4 unfit people, 3: When there are 3 unfit people, 2: When there are 2 unfit people, 1: It is set as "when the unsuitable person is 1 or less".
 衛生教育のリスクの発生頻度には、不適と判定された調査回数の合計が設定される。 The risk occurrence frequency of hygiene education is set to the sum of the number of surveys judged to be unsuitable.
 図18の衛生教育調査結果登録画面の例は、5人の調査対象者のうちの2人目に対する1回の調査結果であるが、5人の調査対象者のうちの2人に対して、不適と判定された調査結果が1回ずつ登録されているとする。この場合、リスク影響度判定部104は、不適者が2人であるので、リスクの影響度を「2」と判定し、リスク発生頻度判定部105は、2人が1回ずつで計2回不適と判定されているので、リスクの発生頻度を「2」と判定する。したがって、安全度算出部106により算出される、衛生教育のリスクの大きさは、2×2=4となる。 The example of the hygiene education survey result registration screen in FIG. 18 is one survey result for the second one of the five survey subjects, but is unsuitable for two of the five survey subjects. It is assumed that the survey results determined to have been registered one by one. In this case, the risk impact determination unit 104 determines that the risk impact is “2” because there are two unqualified persons, and the risk occurrence frequency determination unit 105 is performed twice by two people each. Since the risk is determined to be inappropriate, the risk occurrence frequency is determined to be "2". Therefore, the magnitude of the health education risk calculated by the safety degree calculation unit 106 is 2 × 2 = 4.
 以上をまとめると、それぞれの検査項目および調査項目に対して算出されたリスクの大きさは、以下の通りとなる。
 食中毒細菌(毒素)のリスクの大きさ
  5×5=25
 農薬・抗生物質のリスクの大きさ
  5×5=25
 放射線測定のリスクの大きさ
  1×1=1
 異物混入のリスクの大きさ
  5×4=20
 アレルゲン混入のリスクの大きさ
  5×2=10
 ウイルス検査のリスクの大きさ
  5×3=15
 健康管理のリスクの大きさ
  3×3=9
 感染予防対策のリスクの大きさ
  2×2=4
 身なり・服装・髪型・装飾のリスクの大きさ
  1×1=1
 衛生教育のリスクの大きさ
  2×2=4
Summarizing the above, the magnitude of the risk calculated for each inspection item and investigation item is as follows.
The risk of food poisoning bacteria (toxins) 5 × 5 = 25
The magnitude of the risk of pesticides and antibiotics 5 × 5 = 25
Risk level of radiation measurement 1 × 1 = 1
Risk of contamination 5 x 4 = 20
The risk of allergen contamination 5 × 2 = 10
The magnitude of the risk of virus testing 5 × 3 = 15
Health management risk magnitude 3 × 3 = 9
Risk of infection prevention measures 2 × 2 = 4
The size of the risk of appearance, clothes, hairstyle and decoration 1 × 1 = 1
The magnitude of the risk of hygiene education 2 × 2 = 4
 安全度算出部106は、以上のように算出された各検査項目および各調査項目のリスクの大きさを乗算して、検体のリスクの大きさを算出する。すなわち、安全度算出部106は、次式の計算を行うことにより、検体のリスクの大きさを、2.7×10と算出する。
 25×25×1×20×10×15×9×4×1×4=2.7×10
The degree-of-safety calculation unit 106 calculates the magnitude of the risk of the sample by multiplying the magnitude of the risk of each inspection item and each survey item calculated as described above. That is, the safety degree calculation unit 106 calculates the magnitude of the risk of the sample as 2.7 × 10 8 by performing calculation of the following expression.
25 x 25 x 1 x 20 x 10 x 15 x 9 x 4 x 1 x 4 = 2.7 x 10 8
 そして、検体の安全度は、算出されたリスクの大きさの逆数で与えられるから、安全度算出部106は、以下のように、検体の安全度を算出する。
 検体の安全度=1/(2.7×10)=3.7×10-9
Since the degree of safety of the sample is given by the reciprocal of the magnitude of the calculated risk, the degree-of-safety calculation unit 106 calculates the degree of safety of the sample as follows.
Sample safety = 1 / (2.7 × 10 8 ) = 3.7 × 10 -9
 以上のように、リスク影響度判定部104は、検査結果登録グループおよび調査結果登録グループで登録された検査結果および調査結果に基づいて、検体のリスクの影響度を判定し、リスク発生頻度判定部105は、検査結果登録グループおよび調査結果登録グループで登録された検査結果および調査結果に基づいて、検体のリスクの発生頻度を判定する。そして、安全度算出部106は、算出された各項目のリスクの影響度と、リスクの発生頻度とを用いて、リスクの大きさを算出し、算出されたリスクの大きさから、健康被害に対する安全度を算出する。 As described above, the risk influence degree determination unit 104 determines the degree of influence of the risk of the sample on the basis of the examination result and the examination result registered in the examination result registration group and the examination result registration group. 105 determines the occurrence frequency of the risk of the sample based on the examination result and the examination result registered in the examination result registration group and the examination result registration group. Then, the safety degree calculation unit 106 calculates the magnitude of the risk using the calculated risk impact degree of each item and the frequency of occurrence of the risk, and the magnitude of the calculated risk indicates that the health damage Calculate the degree of safety.
 なお、上述した各項目のリスクの影響度の判定方法、および、リスクの発生頻度の判定方法は、飽くまで一例であり、これに限定されるものではない。 In addition, the determination method of the influence degree of the risk of each item mentioned above, and the determination method of the occurrence frequency of risk are an example until it gets tired, and it is not limited to this.
<安全度算出処理のフローチャート>
 図23のフローチャートを参照して、安全度スケールシステム1による所定の検体の安全度を算出する安全度算出処理について説明する。なお、どの検体の安全度を算出するかは、図23の処理が開始される前に、決定されているものとする。
<Flowchart of safety level calculation process>
The safety degree calculation process for calculating the safety degree of a predetermined sample by the safety degree scale system 1 will be described with reference to the flowchart of FIG. In addition, it is assumed that it is determined before the process of FIG. 23 is started which sample the safety degree is to be calculated.
 初めに、ステップS1において、検査結果登録部102は、算出対象の検体の検査結果登録グループに属する各検査項目の結果を取得する。具体的には、図6の食中毒細菌検査結果登録画面によって入力された検体の食中毒細菌検査の検査結果、図7の農薬・抗生物質検査結果登録画面によって入力された検体の農薬・抗生物質の含有量の検査結果、図11の放射線測定結果登録画面によって入力された検体の放射線量の検査結果、図12の異物混入検査結果登録画面によって入力された検体のアレルゲン混入検査の検査結果、および、図14のウイルス検査結果登録画面によって入力された検体および従事者に対するノロウイルス検査の検査結果が取得される。 First, in step S1, the test result registration unit 102 acquires the result of each test item belonging to the test result registration group of the sample to be calculated. Specifically, the test results of the food poisoning bacteria test of the sample inputted by the food poisoning bacteria test result registration screen of FIG. 6, and the contents of the pesticides / antibiotics of the sample inputted by the pesticides / antibiotics test result registration screen of FIG. Test result of amount, test result of radiation dose of sample inputted by radiation measurement result registration screen of FIG. 11, test result of allergen contamination test of sample inputted by foreign matter contamination test result registration screen of FIG. 12, and The test result of the norovirus test for the specimen and the worker input by the 14 virus test result registration screens is acquired.
 ステップS2において、調査結果登録部103は、算出対象の検体の調査結果登録グループに属する各調査項目の結果を取得する。具体的には、算出対象の検体に対して、図15の健康管理調査結果登録画面によって入力された健康管理の調査結果、図15の健康管理調査結果登録画面によって入力された施設の感染予防対策の調査結果、図17の身なり・服装・髪型・装飾調査結果登録画面によって入力された従事者の身なり・服装・髪型・装飾についての調査結果、および、図18の衛生教育調査結果登録画面によって入力された衛生教育の体制や従事者の理解度についての調査結果が取得される。 In step S2, the survey result registration unit 103 acquires the result of each survey item belonging to the survey result registration group of the sample to be calculated. Specifically, for the sample to be calculated, the infection prevention measures of the facility input by the health management survey result registration screen of FIG. 15 and the health management survey result input by the health management survey result registration screen of FIG. Survey results on the appearance, clothes, hairstyle, decoration of the worker entered by the appearance, clothes, hairstyle, decoration research results registration screen of FIG. 17 and the hygiene education research results registration screen of FIG. 18 The survey results on the health education system and the understanding level of workers are obtained.
 ステップS3において、リスク影響度判定部104は、ステップS1およびステップS2で取得された検査結果および調査結果に基づいて、検査結果または調査結果ごとに、リスクの影響度を判定する。 In step S3, the risk influence degree determination unit 104 determines the degree of risk influence degree for each inspection result or investigation result based on the inspection result and the investigation result acquired in step S1 and step S2.
 ステップS4において、リスク発生頻度判定部105は、ステップS1およびステップS2で取得された検査結果および調査結果に基づいて、検査結果または調査結果ごとに、リスクの発生頻度を判定する。 In step S4, the risk occurrence frequency determination unit 105 determines the occurrence frequency of risk for each test result or check result based on the check result and the check result acquired in step S1 and step S2.
 ステップS5において、安全度算出部106は、検査結果登録グループに属する検査項目または調査結果登録グループに属する調査項目ごとのリスクの大きさを算出する。各検査項目または各調査項目のリスクの大きさは、リスクの影響度とリスクの発生頻度の積で計算される。 In step S5, the safety degree calculation unit 106 calculates the magnitude of the risk for each examination item belonging to the examination result registration group or the examination item belonging to the investigation result registration group. The magnitude of the risk of each test item or each survey item is calculated by the product of the impact of the risk and the frequency of occurrence of the risk.
 ステップS6において、安全度算出部106は、算出された全ての検査項目および調査項目のリスクの大きさを用いて、検体のリスクの大きさを算出する。検体のリスクの大きさは、全ての検査項目および調査項目のリスクの大きさの積で計算される。 In step S6, the safety degree calculation unit 106 calculates the magnitude of the risk of the sample using the calculated magnitudes of the risks of all the test items and the survey items. The magnitude of the risk of the sample is calculated by the product of the magnitude of the risk of all test items and survey items.
 ステップS7において、安全度算出部106は、算出された検体のリスクの大きさを用いて、検体の安全度を算出する。検体の安全度は、算出されたリスクの大きさの逆数で計算される。 In step S7, the safety degree calculation unit 106 calculates the degree of safety of the sample using the calculated magnitude of the risk of the sample. The degree of safety of the sample is calculated by the reciprocal of the calculated magnitude of risk.
 以上で、安全度算出処理は終了する。 This is the end of the safety level calculation process.
 なお、算出された検体の安全度は、登録DB108に記憶され、例えば、図3のメイン画面において、結果一覧ボタン91または結果出力ボタン92が押下された場合など、必要に応じて読み出される。 The calculated degree of safety of the sample is stored in the registration DB 108, and is read out as necessary, for example, when the result list button 91 or the result output button 92 is pressed on the main screen of FIG.
 以上のように、本発明を適用した安全度スケールシステム1は、人間の健康被害に対する安全度(安心度)を、新たな基準で定義し、判定および評価するものである。 As described above, the safety scale system 1 to which the present invention is applied is to define, judge and evaluate the safety (safety) of human health damage based on the new standard.
 安全度スケールシステム1では、人間の健康被害に対する安全度はリスク(危険度)の大きさの裏返しであるとの考えから、人間の健康被害に対する安全度が、算出されたリスクの大きさの逆数で与えられる。 In Safety Level Scale System 1, the safety level against human health damage is the inverse of the calculated risk size, considering that the safety level against human health damage is the reverse of the magnitude of risk (risk level). Given by
 算出された安全度に対応する可視光線波長のカラー色は、例えば、検体(食品)のラベルや包装等に表示されることで、一般の消費者は、ラベルや包装等に表示された安全度を示すカラー色を見るだけで、その食品の安全度を把握することができる。 The color color of the visible light wavelength corresponding to the calculated degree of safety is displayed, for example, on the label or package of the sample (food), so that the general consumer can display the degree of safety displayed on the label or package, etc. By just looking at the color that indicates, you can grasp the degree of safety of the food.
 したがって、算出された安全度の値またはそれに対応するカラー色は、安全度を示す絶対的指標、または、相対的な指標として利用することができる。すなわち、安全度スケールシステム1によれば、健康被害に対する安全度を総合的に判断可能な指標を提供することができる。 Therefore, the value of the calculated degree of safety or the color color corresponding thereto can be used as an absolute index indicating the degree of security or a relative index. That is, according to the safety degree scale system 1, it is possible to provide an index that can comprehensively judge the safety degree against health damage.
 上述した例では、安全度スケールシステム1が、小中学校、工場、オフィス、介護施設などの厨房または食堂、飲食店の店舗、食品工場などの事業所で製造される食品の安全度の検査・評価に適用される例について説明した。 In the example described above, the safety degree scale system 1 inspects and evaluates the degree of safety of food manufactured in elementary or junior high schools, factories, offices, kitchens or cafeterias such as nursing homes, shops of restaurants, food factories etc. An example applied to
 しかし、安全度スケールシステム1は、人間の食する商品(食品)を扱う事業所以外に、農産物・飼料の流通工程や生産工程などにも適用することができ、人間以外に、ペット、家畜等の動物の健康被害に対する安全度(安心度)を検査・評価するシステムとしても利用することができる。 However, safety scale system 1 can be applied to distribution processes and production processes of agricultural products and feeds as well as establishments dealing with products (foods) eaten by humans. It can also be used as a system to inspect and evaluate the degree of safety (reliability) against the health damage of animals.
 なお、本明細書において、システムとは、複数の構成要素(装置、モジュール(部品)等)の集合を意味し、すべての構成要素が同一筐体中にあるか否かは問わない。したがって、別個の筐体に収納され、ネットワークを介して接続されている複数の装置、及び、1つの筐体の中に複数のモジュールが収納されている1つの装置は、いずれも、システムである。 In the present specification, a system means a set of a plurality of components (apparatus, modules (parts), etc.), and it does not matter whether all the components are in the same case. Therefore, a plurality of devices housed in separate housings and connected via a network, and one device housing a plurality of modules in one housing are all systems. .
 本発明の実施の形態は、上述した実施の形態に限定されるものではなく、本発明の要旨を逸脱しない範囲において種々の変更が可能である。 The embodiment of the present invention is not limited to the above-described embodiment, and various modifications can be made without departing from the scope of the present invention.
 例えば、上述した複数の実施の形態の全てまたは一部を組み合わせた形態を採用することができる。 For example, the form which combined all or a part of several embodiment mentioned above is employable.
 例えば、本発明は、1つの機能をネットワークを介して複数の装置で分担、共同して処理するクラウドコンピューティングの構成をとることができる。 For example, the present invention can have a cloud computing configuration in which one function is shared and processed by a plurality of devices via a network.
 また、上述のフローチャートで説明した各ステップは、1つの装置で実行する他、複数の装置で分担して実行することができる。 Further, each step described in the above-described flowchart can be executed by one device or in a shared manner by a plurality of devices.
 さらに、1つのステップに複数の処理が含まれる場合には、その1つのステップに含まれる複数の処理は、1つの装置で実行する他、複数の装置で分担して実行することができる。 Furthermore, in the case where a plurality of processes are included in one step, the plurality of processes included in one step can be executed by being shared by a plurality of devices in addition to being executed by one device.
 1 安全度スケールシステム, 11 サーバ, 12 端末装置, 31 CPU, 32 ROM, 33 RAM, 36 入力部, 37 出力部, 38 記憶部, 39 通信部, 101 基礎情報登録部, 102 検査結果登録部, 103 調査結果登録部, 104 リスク影響度判定部, 105 リスク発生頻度判定部, 106 安全度算出部, 107 結果出力部, 108 登録DB DESCRIPTION OF SYMBOLS 1 Safety degree scale system, 11 server, 12 terminal devices, 31 CPU, 32 ROM, 33 RAM, 36 input part, 37 output part, 38 memory part, 39 communication part, 101 basic information registration part, 102 inspection result registration part, 103 Survey result registration unit, 104 Risk impact degree judgment unit, 105 Risk occurrence frequency judgment unit, 106 Safety degree calculation unit, 107 Result output unit, 108 Registration DB

Claims (7)

  1.  健康被害に対するリスクの影響度を判定する影響度判定部と、
     前記リスクの発生頻度を判定する頻度判定部と、
     判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する安全度算出部と
     を備える情報処理装置。
    An impact determination unit that determines the impact of risk on health damage;
    A frequency determination unit that determines the frequency of occurrence of the risk;
    The degree of safety is calculated by calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk An information processing apparatus comprising:
  2.  前記安全度算出部は、前記健康被害に対する安全度を、算出された前記リスクの大きさの逆数により算出する
     請求項1に記載の情報処理装置。
    The information processing apparatus according to claim 1, wherein the safety degree calculation unit calculates the safety degree with respect to the health damage by a reciprocal of the calculated magnitude of the risk.
  3.  前記安全度算出部により算出された前記安全度に対応した色で、安全度のレベルを出力する安全度出力部をさらに備える
     請求項1または2に記載の情報処理装置。
    The information processing apparatus according to claim 1, further comprising a safety degree output unit that outputs a level of the safety degree with a color corresponding to the safety degree calculated by the safety degree calculation unit.
  4.  前記安全度出力部は、前記安全度の大きさが可視光線の波長に対応するカラー色と対応付けられており、算出された前記安全度に応じた前記可視光線の波長に対応するカラー色で、安全度のレベルを出力する
     請求項3に記載の情報処理装置。
    The safety degree output unit associates the magnitude of the safety degree with a color color corresponding to the wavelength of visible light, and uses a color color corresponding to the wavelength of the visible light according to the calculated safety degree The information processing apparatus according to claim 3, which outputs a level of safety.
  5.  前記影響度判定部は、前記健康被害に対するリスクの影響度を、n段階で判定する
     請求項1乃至3のいずれかに記載の情報処理装置。
    The information processing apparatus according to any one of claims 1 to 3, wherein the influence degree determination unit determines the degree of influence of risk to the health damage in n stages.
  6.  健康被害に対するリスクの影響度を判定し、
     前記リスクの発生頻度を判定し、
     判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する
     ステップを含む情報処理方法。
    Determine the impact of risk on health hazards,
    Determine the frequency of occurrence of the risk,
    Calculating the magnitude of the risk using the determined degree of influence of the risk and the frequency of occurrence of the risk, and calculating the degree of safety against health damage from the magnitude of the calculated risk Information processing method.
  7.  コンピュータに、
     健康被害に対するリスクの影響度を判定し、
     前記リスクの発生頻度を判定し、
     判定された前記リスクの影響度と、前記リスクの発生頻度とを用いて、前記リスクの大きさを算出し、算出された前記リスクの大きさから、健康被害に対する安全度を算出する
     処理を実行させるためのプログラム。
    On the computer
    Determine the impact of risk on health hazards,
    Determine the frequency of occurrence of the risk,
    The magnitude of the risk is calculated using the determined degree of influence of the risk and the frequency of occurrence of the risk, and the process of calculating the degree of safety against health damage from the magnitude of the calculated risk is performed. Program to make
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